Category: 5392-10-9

A variety of minor organobromine compounds are found in nature, but none are biosynthesized or required by mammals. 5392-10-9, formula is C9H9BrO3, Name is 2-Bromo-4,5-dimethoxybenzaldehyde. Organobromine compounds have fallen under increased scrutiny for their environmental impact., Quality Control of 5392-10-9.

Saleem, Faiza;Kanwal;Khan, Khalid Mohammed;Chigurupati, Sridevi;Solangi, Mehwish;Nemala, Appala Raju;Mushtaq, Maria;Ul-Haq, Zaheer;Taha, Muhammad;Perveen, Shahnaz research published 《 Synthesis of azachalcones, their α-amylase, α-glucosidase inhibitory activities, kinetics, and molecular docking studies》, the research content is summarized as follows. Diabetes being a chronic metabolic disorder have attracted the attention of medicinal chemists and biologists. The introduction of new and potential drug candidates for the cure and treatment of diabetes has become a major concern due to its increased prevalence worldwide. In the current study, twenty-seven azachalcone derivatives were synthesized and evaluated for their antihyperglycemic activities by inhibiting α-amylase and α-glucosidase enzymes. Five compounds I (IC₅₀ = 23.08 ± 0.03μM), (IC₅₀ = 26.08 ± 0.43μM), II (IC₅₀ = 24.57 ± 0.07μM), (IC₅₀ = 27.57 ± 0.07μM), III (IC₅₀ = 24.94 ± 0.12μM), (IC₅₀ = 27.13 ± 0.08μM), IV (IC₅₀ = 27.57 ± 0.07μM), (IC₅₀ = 29.13 ± 0.18μM), and V (IC₅₀ = 26.94 ± 0.12μM) (IC₅₀ = 27.99 ± 0.09μM) demonstrated good inhibitory activities against α-amylase and α-glucosidase enzymes, resp. Acarbose was used as the standard in this study. Structure-activity relationship was established by considering the parent skeleton and different substitutions on aryl ring. The compounds were also subjected for kinetic studies to study their mechanism of action and they showed competitive mode of inhibition against both enzymes. The mol. docking studies have supported the results and showed that these compounds have been involved in various binding interactions within the active site of enzyme.

Quality Control of 5392-10-9, 2-Bromo-4,5-dimethoxybenzaldehyde is a useful research compound. Its molecular formula is C9H9BrO3 and its molecular weight is 245.07 g/mol. The purity is usually 95%.
2-Bromo-4,5-dimethoxybenzaldehyde is a synthetic compound that has been shown to be an effective agent for inducing apoptosis in leukemia cells. It is an efficient method for synthesizing the compound and ha2-Bromo-4,5-dimethoxybenzaldehyde induces cell death by topoisomerase-mediated DNA cleavage, which results in chromosomal fragmentation and high levels of reactive oxygen species in the cell., 5392-10-9.

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

Organic bromides such as alkyl bromides are used as fumigants in agriculture to control insects. 5392-10-9, formula is C9H9BrO3, Name is 2-Bromo-4,5-dimethoxybenzaldehyde. Ethylene bromide is one of the commercially important organic bromides which are the component of leaded gasoline. Related Products of 5392-10-9.

Saha, Argha;Guin, Srimanta;Ali, Wajid;Bhattacharya, Trisha;Sasmal, Sheuli;Goswami, Nupur;Prakash, Gaurav;Sinha, Soumya Kumar;Chandrashekar, Hediyala B.;Panda, Sanjib;Anjana, S. S.;Maiti, Debabrata research published 《 Photoinduced Regioselective Olefination of Arenes at Proximal and Distal Sites》, the research content is summarized as follows. Herein, a photoredox catalytic system constituting a merger of palladium/organo-photocatalyst that forges oxidative olefination in an explicit regioselective fashion with diverse arenes and heteroarenes has been established. Visible light plays a significant role in executing ‘regio-resolved’ Fujiwara-Moritani reaction without the requirement of silver salts and thermal energy. The catalytic system is also amenable toward proximal and distal olefination aided by resp. directing groups, which entails the versatility of the protocol in engaging the entire spectrum of C(sp²)-H olefination. Furthermore, streamlining the synthesis of natural products/chiral mols./drugs and diversification through late-stage functionalizations underscore the importance of this sustainable protocol. The photoinduced attainment of this regioselective transformation is mechanistically established through control reactions and kinetic studies.

Related Products of 5392-10-9, 2-Bromo-4,5-dimethoxybenzaldehyde is a useful research compound. Its molecular formula is C9H9BrO3 and its molecular weight is 245.07 g/mol. The purity is usually 95%.
2-Bromo-4,5-dimethoxybenzaldehyde is a synthetic compound that has been shown to be an effective agent for inducing apoptosis in leukemia cells. It is an efficient method for synthesizing the compound and ha2-Bromo-4,5-dimethoxybenzaldehyde induces cell death by topoisomerase-mediated DNA cleavage, which results in chromosomal fragmentation and high levels of reactive oxygen species in the cell., 5392-10-9.

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

Vinyl bromides undergo the Heck reaction, which involves C-C coupling with alkene to give substituted alkenes. 5392-10-9, formula is C9H9BrO3, Name is 2-Bromo-4,5-dimethoxybenzaldehyde. Methyl bromide is a precursor in the manufacture of several chemicals and is employed as a soil sterilant, mainly for seed production. Computed Properties of 5392-10-9.

Rekowski, Szymon P.;Kroener, Bettina K.;Kathuria, Deepika;Wani, Aabid A.;Chourasiya, Sumit S.;Conrad, Juergen;Bharatam, Prasad V.;Frey, Wolfgang;Beifuss, Uwe research published 《 A novel copper-catalyzed, hydrazine-free synthesis of N-1 unsubstituted 1H-indazoles using stable guanylhydrazone salts as substrates》, the research content is summarized as follows. A CuI-catalyzed, hydrazine-free transformation of 2-(2-bromoarylidene)guanylhydrazone hydrochlorides using Cs₂CO₃ as a base and DMEDA as a ligand at 120° for 5 h delivers substituted 1H-indazoles with yields up to 75%. The C,N double bond configuration of the substrates was determined by NMR experiments and quantum chem. calculations The reaction mechanism was studied using quantum chem. calculations

Computed Properties of 5392-10-9, 2-Bromo-4,5-dimethoxybenzaldehyde is a useful research compound. Its molecular formula is C9H9BrO3 and its molecular weight is 245.07 g/mol. The purity is usually 95%.
2-Bromo-4,5-dimethoxybenzaldehyde is a synthetic compound that has been shown to be an effective agent for inducing apoptosis in leukemia cells. It is an efficient method for synthesizing the compound and ha2-Bromo-4,5-dimethoxybenzaldehyde induces cell death by topoisomerase-mediated DNA cleavage, which results in chromosomal fragmentation and high levels of reactive oxygen species in the cell., 5392-10-9.

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

Organic compounds having carbon bonded to bromine are called organic bromides. 5392-10-9, formula is C9H9BrO3, Name is 2-Bromo-4,5-dimethoxybenzaldehyde. Depending on the type of carbon to which the bromine is bonded, organic bromide could be alkyl, alkenyl, alkynyl, or aryl. Electric Literature of 5392-10-9.

Qu, Zhonghua;Tian, Tong;Tan, Yongbo;Ji, Xiaochen;Deng, Guo-Jun;Huang, Huawen research published 《 Redox-neutral ketyl radical coupling/cyclization of carbonyls with N-aryl acrylamides through consecutive photoinduced electron transfer》, the research content is summarized as follows. While the reductive ketyl couplings of carbonyls was widely explored,in this work on a redox-neutral umpolung carbonyl coupling reaction through ketyl radical formation by consecutive photoinduced electron transfer (ConPET) under metal- and additive-free conditions were reported. The donor-acceptor cyanoarene-based fluorophore, 1,2,3,5-tetrakis(carbazol-9-yl)-4,6-dicyanobenzene (4CzIPN), was used as an efficient photocatalyst. It undergoes ConPET to form the excited radical anion (4CzIPN -*) possessing high reductive potential without an external electron donor. This mild and simple photocatalytic system allows highly efficient coupling/cyclization of N-aryl acrylamides and carbonyls and provides straightforward access to structurally useful hydroxyalkyl oxindoles with formal 100% atom economy.

5392-10-9, 2-Bromo-4,5-dimethoxybenzaldehyde is a useful research compound. Its molecular formula is C9H9BrO3 and its molecular weight is 245.07 g/mol. The purity is usually 95%.
2-Bromo-4,5-dimethoxybenzaldehyde is a synthetic compound that has been shown to be an effective agent for inducing apoptosis in leukemia cells. It is an efficient method for synthesizing the compound and ha2-Bromo-4,5-dimethoxybenzaldehyde induces cell death by topoisomerase-mediated DNA cleavage, which results in chromosomal fragmentation and high levels of reactive oxygen species in the cell., Electric Literature of 5392-10-9

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

Organic bromides such as alkyl bromides are used as fumigants in agriculture to control insects. 5392-10-9, formula is C9H9BrO3, Name is 2-Bromo-4,5-dimethoxybenzaldehyde. Ethylene bromide is one of the commercially important organic bromides which are the component of leaded gasoline. Reference of 5392-10-9.

Ramesh, Golla;Ramulu, Bokka Venkat;Balamurugan, Rengarajan research published 《 Activation of o-Propargyl Alcohol Benzaldehydes under Acetalization Conditions for Intramolecular Electrophile Intercepted Meyer-Schuster Rearrangement》, the research content is summarized as follows. The reactivity of o-propargyl alc.-containing benzaldehydes I [R¹ = H, 5-O₂N, 5-MeO, 4,5-(MeO)₂; R² = R³ = Me, Ph; R² = H, R³ = Ph, 4-MeC₆H₄, 1,3-benzodioxol-5-yl, etc.; R² = Me, R³ = Ph, 4-ClC₆H₄, 2-naphthyl, etc.; R² = Ph, R³ = 4-BrC₆H₄, 4-ClC₆H₄, 4-MeC₆H₄] has been increased tremendously toward Bronsted acid-catalyzed intramol. electrophile-intercepted Meyer-Schuster (M-S) rearrangement under acetalization conditions using tri-Me orthoformate. The in situ formed acetal transfers the methoxy group intramolecularly to generate the M-S intermediate in even less reactive substrates, and the formed oxocarbenium ion makes the carbonyl more electrophilic for an effective intramol. trapping of the M-S intermediate to furnish the indanone derivatives II. This procedure was applied to propargyl alc.-functionalized cycloalkenecarboxaldehydes to afford the corresponding cycloalkane-fused (alkylidene)(methoxy)cyclopentenones.

5392-10-9, 2-Bromo-4,5-dimethoxybenzaldehyde is a useful research compound. Its molecular formula is C9H9BrO3 and its molecular weight is 245.07 g/mol. The purity is usually 95%.
2-Bromo-4,5-dimethoxybenzaldehyde is a synthetic compound that has been shown to be an effective agent for inducing apoptosis in leukemia cells. It is an efficient method for synthesizing the compound and ha2-Bromo-4,5-dimethoxybenzaldehyde induces cell death by topoisomerase-mediated DNA cleavage, which results in chromosomal fragmentation and high levels of reactive oxygen species in the cell., Reference of 5392-10-9

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

Organobromine compounds, also called organobromides, are organic compounds that contain carbon bonded to bromine. 5392-10-9, formula is C9H9BrO3, The most pervasive is the naturally produced bromomethane. Recommanded Product: 2-Bromo-4,5-dimethoxybenzaldehyde

Pimparkar, Sandeep;Bhattacharya, Trisha;Maji, Arun;Saha, Argha;Jayarajan, Ramasamy;Dutta, Uttam;Lu, Gang;Lupton, David W.;Maiti, Debabrata research published 《 Para-Selective Cyanation of Arenes by H-Bonded Template》, the research content is summarized as follows. In this work, the para-selective introduction of versatile nitrile moieties RSi(CH(CH₃)₂)₂O(4-R¹C₆H₄) (R = 4-cyanophenoxy, (4-cyanonaphthalen-1-yl)methyl, 2-cyano-10,11-dihydro-5H-dibenzo[a,d]cycloheptene-5-yl, etc.; R¹ = 6-cyano-2H-1,3-benzodioxol-5-yl, 2-(pyridin-3-yl)benzen-1-yl, 2-cyano-4,5-dimethoxybenzen-1-yl, etc.), enabled by a detachable and reusable H-bonded auxiliary was demonstrated. The methodol. holds its efficiency irresp. of substrate electronic bias. The conspicuous shift in the step energetics was probed by both exptl. and computational mechanistic tools, which heralds the inception of para-deuteration. The synthetic impact of the methodol. was highlighted with reusability of directing group and post synthetic modifications.

5392-10-9, 2-Bromo-4,5-dimethoxybenzaldehyde is a useful research compound. Its molecular formula is C9H9BrO3 and its molecular weight is 245.07 g/mol. The purity is usually 95%.
2-Bromo-4,5-dimethoxybenzaldehyde is a synthetic compound that has been shown to be an effective agent for inducing apoptosis in leukemia cells. It is an efficient method for synthesizing the compound and ha2-Bromo-4,5-dimethoxybenzaldehyde induces cell death by topoisomerase-mediated DNA cleavage, which results in chromosomal fragmentation and high levels of reactive oxygen species in the cell., Recommanded Product: 2-Bromo-4,5-dimethoxybenzaldehyde

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

A variety of minor organobromine compounds are found in nature, but none are biosynthesized or required by mammals. 5392-10-9, formula is C9H9BrO3, Name is 2-Bromo-4,5-dimethoxybenzaldehyde. Organobromine compounds have fallen under increased scrutiny for their environmental impact., Application of C9H9BrO3.

Pizova, Hana;Malanik, Milan;Smejkal, Karel;Oravec, Michal;Bobal, Pavel research published 《 Synthesis of C-prenylated analogues of stilbenoid methyl ethers and their cyclic dihydrobenzopyranyl derivatives as potential anti-inflammatory agents》, the research content is summarized as follows. An efficient and versatile synthesis of the naturally occurring C-prenylated stilbenoid Me ethers and their synthetic analogs is presented. The synthesis represents a six step convergent process including an optimized C-prenylation method. Furthermore, during the demethylation process, six new dihydro-benzopyranyl derivatives were obtained and isolated.

Application of C9H9BrO3, 2-Bromo-4,5-dimethoxybenzaldehyde is a useful research compound. Its molecular formula is C9H9BrO3 and its molecular weight is 245.07 g/mol. The purity is usually 95%.
2-Bromo-4,5-dimethoxybenzaldehyde is a synthetic compound that has been shown to be an effective agent for inducing apoptosis in leukemia cells. It is an efficient method for synthesizing the compound and ha2-Bromo-4,5-dimethoxybenzaldehyde induces cell death by topoisomerase-mediated DNA cleavage, which results in chromosomal fragmentation and high levels of reactive oxygen species in the cell., 5392-10-9.

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

Dehydrobromination, Grignard reactions, reductive coupling, Wittig reaction, and several nucleophilic substitution reactions are some of the principal reactions which involve organic bromides. 5392-10-9, formula is C9H9BrO3, Name is 2-Bromo-4,5-dimethoxybenzaldehyde. Organic compounds having carbon bonded to bromine are called organic bromides. Electric Literature of 5392-10-9.

Prasad, Budaganaboyina;Phanindrudu, Mandalaparthi;Nanubolu, Jagadeesh Babu;Kamal, Ahmed;Tiwari, Dharmendra Kumar research published 《 Stereoselective synthesis of (Z)-1,3-bis(α,β-unsaturated carbonyl)-isoindolines from aldehydes and phenacyl azides under metal free conditions》, the research content is summarized as follows. Herein, an unprecedented stereoselective synthesis of 2H-isoindolin-1,3-ylidenes from 2-(formylphenyl)acrylates and phenacyl azide in the presence of piperidine is reported. Unlike in the previous findings, in which 3-keto-isoquinolines were accessed from the same starting materials under slightly modified reaction conditions, this unexpected one-pot tandem reaction allows an efficient and simple method to access a variety of highly functionalized Et (Z)-2-((Z)-3-(2-oxo-2-arylethylidene)-2,3-dihydro-1H-benzo[e]isoindol-1-ylidene)-acetates in very good to excellent yields (up to 91%). The present methodol. is compatible with a wide variety of functional groups.

5392-10-9, 2-Bromo-4,5-dimethoxybenzaldehyde is a useful research compound. Its molecular formula is C9H9BrO3 and its molecular weight is 245.07 g/mol. The purity is usually 95%.
2-Bromo-4,5-dimethoxybenzaldehyde is a synthetic compound that has been shown to be an effective agent for inducing apoptosis in leukemia cells. It is an efficient method for synthesizing the compound and ha2-Bromo-4,5-dimethoxybenzaldehyde induces cell death by topoisomerase-mediated DNA cleavage, which results in chromosomal fragmentation and high levels of reactive oxygen species in the cell., Electric Literature of 5392-10-9

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

Organic compounds having carbon bonded to bromine are called organic bromides. 5392-10-9, formula is C9H9BrO3, Name is 2-Bromo-4,5-dimethoxybenzaldehyde. Depending on the type of carbon to which the bromine is bonded, organic bromide could be alkyl, alkenyl, alkynyl, or aryl. Category: bromides-buliding-blocks.

Phumjan, Tanawat;Songthammawat, Poramate;Jongcharoenkamol, Jira;Batsomboon, Paratchata;Ruchirawat, Somsak;Ploypradith, Poonsakdi research published 《 Substituted 9-Anthraldehydes from Dibenzocycloheptanol Epoxides via Acid-Catalyzed Epoxide Opening/Semipinacol Rearrangement》, the research content is summarized as follows. Starting from benzaldehyde derivatives, the corresponding dibenzocycloheptenol could be prepared in five steps. Under both substrate (secondary vs tertiary alc. and the substituents on the aromatic ring(s)) and condition control, the subsequent epoxidation and acid-catalyzed epoxide opening/semipinacol rearrangement/aromatization afforded the corresponding 9-anthraldehydes in good yields, up to 88% over two steps. The presence of the electron-withdrawing group(s) on the aromatic ring(s) suppressed the rate of the epoxidation while the subsequent semipinacol rearrangement step required heating; the presence of the electron-donating group(s), on the other hand, frequently led to the decomposition during the epoxidation From the mechanistic studies, the semipinacol rearrangement of the epoxide could precede the ionization at the bisbenzylic position, yielding the aldehyde intermediate. The ensuing dehydrative aromatization led to the formation of 9-anthraldehyde. Conversely, nucleophilic addition to the aldehyde and dehydrative aromatization with concomitant loss of formic acid led to anthracene.

Category: bromides-buliding-blocks, 2-Bromo-4,5-dimethoxybenzaldehyde is a useful research compound. Its molecular formula is C9H9BrO3 and its molecular weight is 245.07 g/mol. The purity is usually 95%.
2-Bromo-4,5-dimethoxybenzaldehyde is a synthetic compound that has been shown to be an effective agent for inducing apoptosis in leukemia cells. It is an efficient method for synthesizing the compound and ha2-Bromo-4,5-dimethoxybenzaldehyde induces cell death by topoisomerase-mediated DNA cleavage, which results in chromosomal fragmentation and high levels of reactive oxygen species in the cell., 5392-10-9.

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary

Organic bromides such as alkyl bromides are used as fumigants in agriculture to control insects. 5392-10-9, formula is C9H9BrO3, Name is 2-Bromo-4,5-dimethoxybenzaldehyde. Ethylene bromide is one of the commercially important organic bromides which are the component of leaded gasoline. COA of Formula: C9H9BrO3.

Pan, Wan-Chen;Wang, Yi-Chun;Li, Tuan-Jie;Liu, Jian-Quan;Wang, Xiang-Shan research published 《 An efficient synthesis of 6-benzyl-2-arylthieno[2,3-d]pyrimidin-4(3H)-ones catalyzed by HCl involving a Friedel-Crafts alkylation reaction》, the research content is summarized as follows. Aldehydes could underwent not only the subsequent condensation and cyclization with 2-aminothiophene-3-carboxamides to build a pyrimidine ring, but also a Friedel-Crafts alkylation reaction with thiophene moiety to gave unexpected 6-benzyl-2-arylthieno[2,3-d]pyrimidin-4(3H)-ones I [R¹ = H, Cl, F, Me, MeO; R² = H, Cl, F, MeO; Ar = Ph, 4-MeC₆H₄, 4-EtC₆H₄, 4-n-PrC₆H₄, 4-ClC₆H₄] and II [R³ = 2-MeOC₆H₄, 2-Br-4-FC₆H₃, 2-furyl, etc.] in good yields catalyzed by concentrated HCl.

COA of Formula: C9H9BrO3, 2-Bromo-4,5-dimethoxybenzaldehyde is a useful research compound. Its molecular formula is C9H9BrO3 and its molecular weight is 245.07 g/mol. The purity is usually 95%.
2-Bromo-4,5-dimethoxybenzaldehyde is a synthetic compound that has been shown to be an effective agent for inducing apoptosis in leukemia cells. It is an efficient method for synthesizing the compound and ha2-Bromo-4,5-dimethoxybenzaldehyde induces cell death by topoisomerase-mediated DNA cleavage, which results in chromosomal fragmentation and high levels of reactive oxygen species in the cell., 5392-10-9.

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary