Author: Jessica.F

Jimoh, Tajudeen A. published the artcileBiological evaluation and docking study of synthesized derivatives of benzotriazole and benzimidazole as antibacterial agents, Product Details of C8H17Br, the publication is Chemistry Africa (2022), 5(3), 509-523, database is CAplus.

To tackle the menace of multi-resistant bacteria which pose challenges to scientist, four benzotriazole derivatives and three benzimidazole derivatives were synthesized via two routes due to the importance of heterocyclic compound in medicinal chem. Two protein target DNA gyrase with PDB ID 2XCT and PDB ID 3ILW were docked with the synthesized compound and compared with the two standard drugs sparfloxacin and ciprofloxacin. For benzotriazole derivatives, the reaction in acetonitrile resulted in lower yields (18-25%) than with dimethylformamide/potassium hydroxide (DMF/KOH), which generated higher yields (68-92%) in shorter reaction time. Those of benzimidazole were comparable. The products were characterized by FTIR, 1H, and 13C NMR, while the association between atoms was shown in 2D NMR. The synthesized compounds were docked against two DNA gyrase with PDB ID 2XCT and PDB ID 3ILW. It was observed that 1-butyl-1H-benzotriazole (- 13.716) and 1-butyl-3-octyl-1H-benzotriazolium (- 12.324) were the most active against PDB ID 2XCT and PDB ID 3ILW, resp. However, they were both less active than the standard drugs used. Using the agar diffusion technique, the synthesized compounds demonstrated broad-spectrum antibacterial activity against gram-pos. and gram-neg. pathogenic bacteria strains. Notably, all the compounds were of varying potency; with inhibition zones ranging from 24 to 30 mm and MIC ranging from 25 to 50 μg/mL. The benzotriazole and benzimidazole derivatives were synthesized successfully. This research revealed that the synthesized compounds were active against organisms with activity, the docking results revealed that the synthesized compounds have relatively low binding energy when compared with the standard drug used as well as those reported earlier. Thus, it will give better interaction on the binding site of the protein. These synthesized compounds could be a source of new drugs that could be used to treat multi-resistance bacteria.

Chemistry Africa published new progress about 111-83-1. 111-83-1 belongs to bromides-buliding-blocks, auxiliary class Bromide,Aliphatic hydrocarbon chain, name is 1-Bromooctane, and the molecular formula is C8H17Br, Product Details of C8H17Br.

Referemce:
https://en.wikipedia.org/wiki/Bromide,
bromide – Wiktionary

Miura, Yozo published the artcileMagnetic Interaction of Pyridyl-Substituted Thioaminyl Stable Free Radicals, Name: Mono(N,N,N-trimethyl-1-phenylmethanaminium) tribromide, the publication is Journal of Organic Chemistry (2003), 68(4), 1225-1234, database is CAplus and MEDLINE.

N-(2-Pyridylthio)-2,6-diaryl-4-R-phenylaminyls (R = Ph, 4-ClC₆H₄, MeCO, CN, EtOCO) and N-(4-pyridylthio)-2,6-diaryl-4-R-phenylaminyls (R = Ph, 4-ClC₆H₄, EtOCO) were prepared and isolated as radical crystals. Their ESR spectra were measured, and the NS and pyridyl N and anilino meta and pyridyl ortho and para proton hyperfine coupling constants were determined The spin-d. calculations based on the d. functional theory were performed by the UBecke 3LYP hybrid method using the STO 6-31G basis set. x-ray crystallog. analyses were performed for three radicals, and their structures were discussed. The magnetic susceptibility measurements were carried out for the nine kinds of isolated radicals with a SQUID magnetometer. One radical showed ferromagnetic coupling (2J/k_B = 44 K), and the others showed antiferromagnetic behavior. The magnetic interactions observed are explained from the crystal structures.

Journal of Organic Chemistry published new progress about 111865-47-5. 111865-47-5 belongs to bromides-buliding-blocks, auxiliary class Benzenes, name is Mono(N,N,N-trimethyl-1-phenylmethanaminium) tribromide, and the molecular formula is C10H16Br3N, Name: Mono(N,N,N-trimethyl-1-phenylmethanaminium) tribromide.

Referemce:
https://en.wikipedia.org/wiki/Bromide,
bromide – Wiktionary

Zheng, Hai-jin published the artcileSynthesis and property of a new type of chromogenic reagent of thiazolylazo, Name: Sodium 3-bromopropane-1-sulfonate, the publication is Huaxue Yanjiu (2004), 15(3), 42-44, database is CAplus.

The synthesis of 2-(4,5-dimethyl-2-thiazoleazo)-4-methyl-5-sulfopropylaminobenzoic acid is reported. Its chromogenic property with Cu²⁺, Ni²⁺, Co²⁺ was studied. It can form stable compounds with Cu²⁺, Ni²⁺, Co²⁺. The maximum absorptions of these compounds are at 628 nm, 590 run, 583 nm, and their molar absorptivities (ε) are 8.4 × 10⁴, 5.8 × 10⁴ and 4.8 × 10⁴, resp. Also this material can be used as a good spectrophotometric chromogenic agent for some metal ions.

Huaxue Yanjiu published new progress about 55788-44-8. 55788-44-8 belongs to bromides-buliding-blocks, auxiliary class Bromide,Salt,Aliphatic hydrocarbon chain,Aliphatic hydrocarbon chain, name is Sodium 3-bromopropane-1-sulfonate, and the molecular formula is C15H14O3, Name: Sodium 3-bromopropane-1-sulfonate.

Referemce:
https://en.wikipedia.org/wiki/Bromide,
bromide – Wiktionary

Woolfe, G. published the artcileTrypanocidal action of phenanthridine compounds: effect of changing the quaternary groups of known trypanocides, Safety of Dimidium bromide, the publication is British Journal of Pharmacology and Chemotherapy (1956), 330-3, database is CAplus and MEDLINE.

cf. Ann. Trop. Med. Parasitol. 46, 285(1952). The effect on trypanocidal activity of replacing the Me quaternating group of 6-(4-aminophenyl)-8-aminophenanthridinium halide and 3,8-diamino-6-alkyl (or aryl)-phenanthridinium halide with Et, Pr, or allyl was examined Trypanocidal activity measured against Trypanosoma congolense, T. brucei, T. rhodesiense, and T. gambiense was generally enhanced and was greatest with compounds originally of high activity. Toxicities for mice were also reported.

British Journal of Pharmacology and Chemotherapy published new progress about 518-67-2. 518-67-2 belongs to bromides-buliding-blocks, auxiliary class Other Aromatic Heterocyclic,Salt,Amine,Benzene, name is Dimidium bromide, and the molecular formula is C28H29NO4, Safety of Dimidium bromide.

Referemce:
https://en.wikipedia.org/wiki/Bromide,
bromide – Wiktionary

Wohl, A. published the artcileBromination of unsaturated compounds with N-bromoacetamide, a contribution to the study of the course of chemical processes, Computed Properties of 594-81-0, the publication is Berichte der Deutschen Chemischen Gesellschaft [Abteilung] B: Abhandlungen (1919), 51-63, database is CAplus.

It has now become quite widely accepted that substitution reactions are often preceded by addition reactions and the present investigation was carried out in the course of a search for reactions which would make it possible to decide with certainty whether there is really a primary addition and, if so, whether it is molecular or atomic. W. found, e. g., that the reaction Me₂C:CMe₂ + AcNHBr (a) → Me₂C:CMeCH₂Br + AcNH₂ occurs under such conditions (good cooling in Et₂O or Me₂CO) that the (a) is not dissociated at all or only to a very minute extent; no HBr can be detected. This reaction can in no way be explained as taking place by addition of the residues Br and AcNH of the (a) to the two C atoms of the double bond, for an acetylated bromoamine would split off HBr and not AcNH₂. Moreover, the behavior of (a) towards Me₂C:CHMe (see below) also shows that the Br does not combine with either of the unsaturated C atoms. There, therefore, remains but one possibility, that the primary addition occurs through subsidiary valences on (a) and one or both of the trivalent C atoms and the resulting unstable structure with the loosest union between Br and N then loses AcNH, forming AcNH₂ with the most labile H atom after the Br and this H atom, obeying the law of neutralization, have exchanged places. According to W.’s views, the high additive power of (a) depends on the union, the spatial proximity, of the two fields of affinity of the unsaturated negative atoms -NBr, just like H₂N.OH, H₂N.NH₂, HO.NO, (HO)₂SO, HN:C, etc. Compounds without this union, like the hydrazonium salts, H₂NNMe₃I, are quite indifferent, e. g., towards aldehydes. Me₂C:CHMe and (a) under such conditions (sufficient dilution and cooling) that AcNH₂ seps. and the Br derivative remains in solution give exclusively a di-Br compound C₅H₈Br₂. If, however, equimol. amounts of Me₂C:CHMe and (a) are brought together in cold Et₂O they combine and sep. practically quant. as an oil which, when the Et₂O is poured off, undergoes an energetic reaction just like when Me₂C:CHMe and (a) are brought together without a diluent. It is, therefore, not the addition product stable at low temperatures which determines the course of the substitution reaction but some part of it (which could not be isolated) in the mixture formed when the temperature is raised. In the substitution reaction it is one of the primary H atoms, not the tertiary atom, which is replaced. The primary addition is, therefore, determined by the coóperation of the Br-N secondary valences and the C double bond, and the further course of the reaction by the mobility of the H atoms; according to the well-known rule, the double bond loosens the H on the adjacent C atom. In harmony with these views it was found that (a) does not attack compounds saturated in the usual sense (except Me₃CBr) and a series of compounds unsaturated in the ordinary sense but lacking the conditions of easy addition or of mobile H atoms (EtBr, iso-PrBr, (CH₂Br)₂, PhCH₂Br and CH₂(CO₂Et)₂ in the first group and C₂H₄, C₂H₂, maleic and fumaric acids, PhCH:CHCO₂H, PhCH:CHCO₂Et and PhCH:CHCHO in the second group). Malonic ester, in spite of the mobile H atoms, lacks a grouping appropriate for the primary addition; this, however, is present in the derivative EtO₂CCH₂CONH₂ which in Me₃CO smoothly forms the compound EtO₂CCHBrCONH₂, the transient yellow color appearing during the course of its preparation indicating the formation of a Br-N compound with pentavalent N in which the migration of the Br from N to C occurs by intramol. substitution. The indifference of the other compounds of the second group is easily explained by the absence of a reactively influenced H atom. On the other hand, AcCH₂CO₂Et, PhOH and, to a less marked degree, PhOMe react with (a) just like Me₂C:CMe₂ and Me₂C:CHMe. The same is true of Me₃CBr, PhCH:CH₂, MeCH:CHCO₂H, NCCH₂CO₂Et, AcH, HCO₂H and HCO₂Et. The (a) used was recrystallized from C₆H₆, m. 108° and was colorless; as diluents were used Et₂O (in which it is not soluble but dissolves as the reaction proceeds and AcNH₂ seps.) or Me₂CO which dissolves (a) readily without being itself markedly brominated in the cold. In general, as soon as the starch-iodide reaction was no longer given, the AcNH₂, was removed, after addition of Et₂O, by shaking with Na₂CO₃ and washing with H₂O and the H₂O-insoluble layer was dried with Na₂SO₄ and fractionated in vacuo. Without a diluent (a) acts on easily brominated compounds with much evolution of heat, darkening and violent decomposition, the unattacked (a) itself being thereby decomposed with liberation of Br. From 10 g. cold Me₂C:CHMe treated with four 10-g. portions of (a) in 60 cc. Me₂CO was obtained 9 g. of a compound, C₅H₈Br₂ (b) (found 69.74% Br; calculated, 70.14), b₁₂ 54-5°, decolorizes KMnO₄ and Br-H₂O in alc.; no mono-Br derivative is formed, even when a large excess of Me₂C:CHMe is used (20 g. to 20 of Br). Me₂C:CBrMe, prepared by Bauer’s method (Bull. soc. chim. 2, 149(1860)) but from pure Me₂C:CHMe instead of amylene, b₇₆₆ 119-20°; it reacts much more slowly than Me₂C:CHMe with (a); 14.9 g. added at room temperature to 13.8 g. (a) in 60 cc. Me₂CO and allowed to stand 24 hrs. without cooling, gave, besides unchanged Me₂C:CBrMe, a fraction b₂₅ 96-8° with 69.43% Br. This dibromotrimethylethylene partly polymerizes on cooling and unlike (b) has an intense odor and attacks the eyes. From 10 g. Me₂C:CMe₂ in 36 cc. cold Et₂O and 16 g. (a) is obtained about 3 g. of not quite pure bromotetramethylethylene (found 46.3% Br; calculated 49.0%), b₁₅, 60-90°, decolorizes KMnO₄, easily decomposes and polymerizes. Me₃CBr (37 g.) in 10 cc. cold Et₂O slowly treated with 37 g. (a) yields 7 g. Me₂C(CH₂Br)Br, b₃₆ 60-1°, b. 149°. From 44.3 g. PhOH in 145 cc. cold Et₂O treated at 12 hr. intervals With, 20, 20 and 25 g. (a) is obtained p-BrC₆H₄OH, m. 64°, b₂₁ 1.39°, b, 236°. PhOMe (10.8 g.) and 13.8 g. (a) in 65 cc. Me₂CO after 24 hrs. at room temperature gave 17 g. p-BrC₆H₄OMe, m. 11-1.5°, b. 215°. AcCH₂CO₂Et (21.7 g.) in 100 cc. cold Et₂O treated in the course of 1 day with 8 + 8 + 7 g. (a) yields 15 g. AcCHBrCO₂Et, b₁₈ 106-8°. From 2 g. EtO₂CCH₂CONH₂ (prepared by heating EtO₂CCH₂C(OEt):NH.HCl at 125-30°) in 5 cc. cold Me₂CO, slowly treated with 2 g. (a) in 5 cc. Me₂CO and allowed to stand 24 hrs. to disappearance of the yellow color and the starch-iodide reaction, is obtained a mixture of AcNH₂ and EtO₂CCHBrCONH₂

Berichte der Deutschen Chemischen Gesellschaft [Abteilung] B: Abhandlungen published new progress about 594-81-0. 594-81-0 belongs to bromides-buliding-blocks, auxiliary class Bromide,Aliphatic hydrocarbon chain, name is 2,3-Dibromo-2,3-dimethylbutane, and the molecular formula is C19H24BNO2, Computed Properties of 594-81-0.

Referemce:
https://en.wikipedia.org/wiki/Bromide,
bromide – Wiktionary

Wien, R. published the artcileChemotherapeutic action of amidine and phenanthridinium compounds in Trypanosoma congolense infections, SDS of cas: 518-67-2, the publication is British Journal of Pharmacology and Chemotherapy (1946), 65-80, database is CAplus and MEDLINE.

These compounds were tested against 5 strains of T. congolense in mice: 7-Amino-9-p-aminophenyl-10-methylphenanthridinium chloride and 4,4′-diamidino-α,β-dimethylstilbene di-HCl were compared as to activity. The former compound was twice as toxic and active against the acute strains, the therapeutic indexes being the same, but it was less active against 1 chronic strain. An evaluation of 2,7-diamino-9-phenyl-10-methyl-phenanthridinium bromide (1553) showed that by subcutaneous injection in acute infections the C.D. 50(50% of animals free of trypanosomes for at least 28 days, 42 for chronic strains) was 0.0004 mg./g., the LD 50 was 0.061 mg./g. and the therapeutic index 152. A very complete study of the correlation between chem. structure and activity against T. congolense of diamidine and phenanthridinium compounds is reported. The pharmacol. actions of compound 1553 are reported. The compound has a depressant action on the circulation and respiratory center and, in high doses, a toxic action on liver and kidneys.

British Journal of Pharmacology and Chemotherapy published new progress about 518-67-2. 518-67-2 belongs to bromides-buliding-blocks, auxiliary class Other Aromatic Heterocyclic,Salt,Amine,Benzene, name is Dimidium bromide, and the molecular formula is C17H14F3N3O2S, SDS of cas: 518-67-2.

Referemce:
https://en.wikipedia.org/wiki/Bromide,
bromide – Wiktionary

Wang, Ya-zhen published the artcileSynthesis of 5-bromo-1-methyl-2-phenyl-1H-benzimidazole, Safety of 4-Bromo-N-methyl-2-nitroaniline, the publication is Huaxue Yanjiu Yu Yingyong (2015), 27(11), 1721-1725, database is CAplus.

5-Bromo-1-methyl-2-phenyl-1H-benzimidazole was intermediate to prepare anti-cancer pharmaceuticals, and organic electroluminescence devices. The key intermediate N-(4-bromo-2-nitrophenyl)-N-methylbenzamide was prepared using N-methyl-2-nitroaniline as starting material which was consisted of benzene ring bromination, N-benzoylation reaction, following with reaction of nitroredn. and closed ring reaction of intramolecularly dehydration. The target product 5-bromo-1-methyl-2-phenyl-1H-benzimidazole (I) was synthesized in excellent yield. The chem. structures were characterized by ¹H-NMR, ¹³C-NMR and IR, and purity was determined by HPLC.

Huaxue Yanjiu Yu Yingyong published new progress about 53484-26-7. 53484-26-7 belongs to bromides-buliding-blocks, auxiliary class Bromide,Nitro Compound,Amine,Benzene, name is 4-Bromo-N-methyl-2-nitroaniline, and the molecular formula is C9H6BrNO, Safety of 4-Bromo-N-methyl-2-nitroaniline.

Referemce:
https://en.wikipedia.org/wiki/Bromide,
bromide – Wiktionary

Sysoeva, N. D. published the artcileThe application of the Chugaev xanthic reaction to secondary-tertiary and ditertiary glycols. II. Experimental part. The effect of sodium xanthate on trimethylethylene dibromide, Safety of 2,3-Dibromo-2,3-dimethylbutane, the publication is Trudy Uzbekskogo Inst. Narodnogo Khoz. (1940), 1-11, database is CAplus.

The heating of the dibromides of the tri- and tetramethylethylenes with Na xanthate on a water bath at 60-70° resulted in the formation of tri- and tetramethylethylenes the separation and identification of which are described in detail. Through Khim. Referat. Zhur. 4, Number 7-8, 40-1(1941).

Trudy Uzbekskogo Inst. Narodnogo Khoz. published new progress about 594-81-0. 594-81-0 belongs to bromides-buliding-blocks, auxiliary class Bromide,Aliphatic hydrocarbon chain, name is 2,3-Dibromo-2,3-dimethylbutane, and the molecular formula is C12H15NO, Safety of 2,3-Dibromo-2,3-dimethylbutane.

Referemce:
https://en.wikipedia.org/wiki/Bromide,
bromide – Wiktionary

Streitwieser, Andrew Jr. published the artcileThe application of Taft’s equation to polar effects in solvolyses, Application In Synthesis of 594-81-0, the publication is Journal of the American Chemical Society (1956), 4935-8, database is CAplus.

The Taft equation, log (k/k₀) = σ*ρ* (cf. C.A. 48, 11888f), was applied to the solvolysis of secondary carbinyl sulfonates in AcOH, of tertiary halides in aqueous EtOH, and of primary tosylates in EtOH, with satisfactory results. Driving forces for anchimeric assistance are derived from the correlations.

Journal of the American Chemical Society published new progress about 594-81-0. 594-81-0 belongs to bromides-buliding-blocks, auxiliary class Bromide,Aliphatic hydrocarbon chain, name is 2,3-Dibromo-2,3-dimethylbutane, and the molecular formula is C10H15ClO3S, Application In Synthesis of 594-81-0.

Referemce:
https://en.wikipedia.org/wiki/Bromide,
bromide – Wiktionary

Stallberg, Gunnel published the artcilePreparation of half-esters of alkylsuccinic acids with a free primary carboxyl group. Synthesis and optical configuration of optically active methyl 2-methyl-3-carboxypropanoate, Name: 3-Bromo-2-methylpropanoic acid, the publication is Acta Chemica Scandinavica (1956), 1360-1, database is CAplus.

The preparation of HO₂CCH₂CHMeCO₂Me (I), m. 42.2-2.8° (petr. ether), n²⁶_D 1.4309, [α]²⁵_D -9.3° (c 17.5, CHCl₃), made difficult by the simultaneous formation of HO₂CCHMeCH₂CO₂Me, is achieved in 60-8% yield by distilling the KMnO₄ oxidation product of CH₂:CHCH₂CHMeCO₂Me, b₇₆₀ 134.5-5.0°, n^22.6_D 1.4158, [α]²²_D 17.0°, without partial racemization (in contrast to the oxidation of optically active CH₂:CHCH₂CHMeCO₂H with H₂CrO₄). Using Hunsdiecker’s procedure (C.A. 37, 3734⁴) I is converted into BrCH₂CHMeCO₂Me, [α]²⁴_D 13.8°, which on hydrolysis with HBr in glacial AcOH gives BrCH₂CHMeCO₂H, [α]²⁷_D 10.1° (c 14.4, CHCl₃).

Acta Chemica Scandinavica published new progress about 56970-78-6. 56970-78-6 belongs to bromides-buliding-blocks, auxiliary class Bromide,Carboxylic acid,Aliphatic hydrocarbon chain,Inhibitor, name is 3-Bromo-2-methylpropanoic acid, and the molecular formula is C4H3Cl2N3, Name: 3-Bromo-2-methylpropanoic acid.

Referemce:
https://en.wikipedia.org/wiki/Bromide,
bromide – Wiktionary