2-溴苯乙酮

一般危化品
2-溴苯乙酮结构式
2-溴苯乙酮结构式
常用名 2-溴苯乙酮 英文名 2-Bromoacetophenone
CAS号 70-11-1 分子量 199.045
密度 1.5±0.1 g/cm3 沸点 253.4±0.0 °C at 760 mmHg
分子式 C8H7BrO 熔点 48-51 °C(lit.)
MSDS 中文版 美版 闪点 78.4±7.2 °C
符号 GHS05
GHS05
信号词 Danger

Structure-activity relationships of a novel pyranopyridine series of Gram-negative bacterial efflux pump inhibitors.

Bioorg. Med. Chem. 23(9) , 2024-34, (2015)

Recently we described a novel pyranopyridine inhibitor (MBX2319) of RND-type efflux pumps of the Enterobacteriaceae. MBX2319 (3,3-dimethyl-5-cyano-8-morpholino-6-(phenethylthio)-3,4-dihydro-1H-pyrano[3,4-c]pyridine) is structurally distinct from other known G...

Nucleophilic heterocyclic carbene as a novel catalyst for cyclopropanation of cyano acrylates.

Org. Biomol. Chem. 8(4) , 901-5, (2010)

Nucleophilic heterocyclic carbenes (NHCs) have been used for the first time as catalysts in the cyclopropanation of ethyl cyanocinnamates with phenacyl bromide by Michael-initiated ring-closure (MIRC).

Bromoacetophenone-based photonucleases: photoinduced cleavage of DNA by 4'-bromoacetophenone-pyrrolecarboxamide conjugates.

Org. Lett. 1(13) , 2117-20, (1999)

[formula: see text] 4'-Bromoacetophenone derivatives which upon excitation can generate monophenyl radicals capable of hydrogen atom abstraction were investigated as photoinducible DNA cleaving agents. Pyrrolecarboxamide-conjugated 4'-bromoacetophenones were ...

A convenient ultrasound-promoted synthesis of some new thiazole derivatives bearing a coumarin nucleus and their cytotoxic activity.

Molecules 17(8) , 9335-47, (2012)

Successful implementation of ultrasound irradiation for the rapid synthesis of a novel series of 3-[1-(4-substituted-5-(aryldiazenyl)thiazol-2-yl)hydrazono)ethyl]-2H-chromen-2-ones 5a-h, via reactions of 2-(1-(2-oxo-2H-chromen-3-yl)ethylidene) thiosemicarbazi...

Synthesis and biological activities of new substituted thiazoline-quinoline derivatives.

Acta. Pharm. 59(4) , 365-82, (2009)

5-Acyl-8-hydroxyquinoline-2-(3'-substituted-4'-aryl-2,3-dihydrothiazol-2'-ylidene)hydrazones, 5a-e to 10a-c, were prepared by the reaction of appropriate 5-acyl-8-hydroxyquinoline-4-substituted thiosemicarbazones 3a-e and phenacyl bromides 4a-e. Structures of...

alpha-bromoacetophenone derivatives as neutral protein tyrosine phosphatase inhibitors: structure-Activity relationship.

Bioorg. Med. Chem. Lett. 12(21) , 3047-50, (2002)

A series of alpha-haloacetophenone derivatives was tested for inhibition of protein tyrosine phosphatases SHP-1 and PTP1B. The results show that the bromides are much more potent than the corresponding chlorides, whereas the phenyl ring is remarkably tolerant...

FT-IR and FT-Raman spectral investigation, computed IR intensity and Raman activity analysis and frequency estimation analysis on 4-chloro-2-bromoacetophenone using HF and DFT calculations.

Spectrochim. Acta. A. Mol. Biomol. Spectrosc. 78(2) , 826-34, (2011)

In this work, the experimental and theoretical spectra of 4-chloro-2-bromoacetophenone (4C2BAP) are studied. FT-IR and FT-Raman spectra of title molecule have been recorded in the region 4000-100 cm(-1). The structural and spectroscopic data of the molecule i...

High-performance liquid chromatographic determination of cytosine-containing compounds by precolumn fluorescence derivatization with phenacyl bromide: application to antiviral nucleosides and nucleotides.

J. Chromatogr. B, Biomed. Appl. 679(1-2) , 119-27, (1996)

A novel precolumn derivatization method for the HPLC determination of cytosine-containing compounds by HPLC is described. Highly fluorescent 2-phenyl-3,N4-ethenocytosine derivatives are produced by a reaction of non-fluorescent cytosine-containing compounds w...

Measurement of plasma acetate kinetics using high-performance liquid chromatography.

Anal. Biochem. 198(1) , 149-53, (1991)

Previous studies suggest that plasma acetate may be an important fuel in man, accounting for approximately 10% of energy expenditure. Available methods for the determination of plasma acetate kinetics are difficult and time consuming. We describe here a proce...

Active-site residues of procarboxypeptidase Y are accessible to chemical modification.

Biochim. Biophys. Acta 1205(2) , 289-93, (1994)

The accessibility of the active-site cleft of procarboxypeptidase Y from Saccharomyces cerevisiae has been studied by chemical modifications of two specific amino-acid residues. Previous studies have shown that these residues, Cys-341 and Met-398 in the matur...