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2-BROMO-1-(2-PHENOXYPHENYL)ETHANONE, also known as 2-Bromoacetophenone, is an organic compound belonging to the acetophenone family. It is a white solid with a molecular formula C14H11BrO and a molecular weight of 271.14 g/mol. This versatile chemical is widely used in the synthesis of pharmaceuticals and agrochemicals, serving as a crucial intermediate in the production of other organic compounds. Additionally, it has been studied for its potential biological and pharmacological activities, including antiallergic and anti-inflammatory properties. However, it is essential to handle this chemical with care due to its potential health hazards upon exposure.

94402-42-3

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94402-42-3 Usage

Uses

Used in Pharmaceutical Industry:
2-BROMO-1-(2-PHENOXYPHENYL)ETHANONE is used as a key intermediate in the synthesis of various pharmaceuticals for its ability to contribute to the development of new drugs and improve the efficacy of existing ones.
Used in Agrochemical Industry:
2-BROMO-1-(2-PHENOXYPHENYL)ETHANONE is used as a building block in the production of agrochemicals, helping to create effective solutions for pest control and crop protection.
Used in Organic Chemistry Research:
2-BROMO-1-(2-PHENOXYPHENYL)ETHANONE is used as a versatile compound in organic chemistry research for its potential to form new chemical entities and contribute to the advancement of chemical science.
Used in Biological and Pharmacological Studies:
2-BROMO-1-(2-PHENOXYPHENYL)ETHANONE is used as a subject of study in biological and pharmacological research for its potential antiallergic and anti-inflammatory properties, aiming to develop new therapeutic agents and treatments.

Check Digit Verification of cas no

The CAS Registry Mumber 94402-42-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,4,4,0 and 2 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 94402-42:
(7*9)+(6*4)+(5*4)+(4*0)+(3*2)+(2*4)+(1*2)=123
123 % 10 = 3
So 94402-42-3 is a valid CAS Registry Number.
InChI:InChI=1/C14H11BrO2/c15-10-13(16)12-8-4-5-9-14(12)17-11-6-2-1-3-7-11/h1-9H,10H2

94402-42-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Bromo-1-(2-phenoxyphenyl)ethanone

1.2 Other means of identification

Product number -
Other names 2-BROMO-1-(2-PHENOXYPHENYL)ETHANONE

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:94402-42-3 SDS

94402-42-3Relevant academic research and scientific papers

CYANO-SUBTITUTED HETEROCYCLES WITH ACTIVITY AS INHIBITORS OF USP30

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Page/Page column 48; 49, (2018/04/17)

The present invention relates to a class of cyano-substituted-heterocycles of Formula (I) with activity as inhibitors of deubiquitilating enzymes, in particular, ubiquitin C-terminal hydrolase 30 or ubiquitin specific peptidase 30 (USP30), having utility in a variety of therapeutic areas including cancer and conditions involving mitochondrial dysfunction. (I)

2- and 3-substituted imidazo[1,2-a]pyrazines as inhibitors of bacterial type IV secretion

Sayer, James R.,Walldn, Karin,Pesnot, Thomas,Campbell, Frederick,Gane, Paul J.,Simone, Michela,Koss, Hans,Buelens, Floris,Boyle, Timothy P.,Selwood, David L.,Waksman, Gabriel,Tabor, Alethea B.

, p. 6459 - 6470 (2015/01/09)

A novel series of 8-amino imidazo[1,2-a]pyrazine derivatives has been developed as inhibitors of the VirB11 ATPase HP0525, a key component of the bacterial type IV secretion system. A flexible synthetic route to both 2- and 3-aryl substituted regioisomers has been developed. The resulting series of imidazo[1,2-a]pyrazines has been used to probe the structure-activity relationships of these inhibitors, which show potential as antibacterial agents.

SUBSTITUTED 8 - AMINO - IMIDAZO [1, 2-A] PYRAZ1NES AS ANTIBACTERIAL AGENTS

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Page/Page column 42-43, (2013/02/27)

The present invention relates to substituted imidazo[1,2-a]pyrazines of Formula (I) and their use as antibacterial agents.

Pyrrolo[2,3-d]pyrimidines containing an extended 5-substituent as potent and selective inhibitors of lck I

Arnold, Lee D.,Calderwood, David J.,Dixon, Richard W.,Johnston, David N.,Kamens, Joanne S.,Munschauer, Rainer,Rafferty, Paul,Ratnofsky, Sheldon E.

, p. 2167 - 2170 (2007/10/03)

Pyrrolo[2,3-d]pyrimidines containing a 5-(4-phenoxyphenyl) substituent are potent and selective inhibitors of lck in vitro; some compounds are selective for lck over src. Data are shown for two compounds demonstrating that they are potent and selective in

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