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1-(4-Bromo-3-chlorophenyl)ethanone is a chemical compound characterized by the molecular formula C8H6BrClO. It is a yellow solid substance that plays a significant role in organic synthesis and pharmaceutical research. As a ketone derivative, it features a carbonyl group attached to two hydrocarbon groups, which contributes to its versatility in chemical reactions and applications.

3114-31-6

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3114-31-6 Usage

Uses

Used in Pharmaceutical Research:
1-(4-Bromo-3-chlorophenyl)ethanone is utilized as an intermediate in the production of various pharmaceuticals. Its unique structure allows it to be a key component in the synthesis of complex molecules, making it valuable for researchers and chemists in the development of new compounds for medical applications.
Used in Agrochemical Production:
1-(4-Bromo-3-chlorophenyl)ethanone also serves as an intermediate in the creation of agrochemicals, contributing to the development of products that enhance agricultural productivity and crop protection.
Used in Organic Chemistry:
1-(4-Bromo-3-chlorophenyl)ethanone is applied in the field of organic chemistry for the synthesis of intricate organic molecules. Its structural properties are crucial for advancing scientific research and the creation of novel compounds for a wide range of industrial applications.

Check Digit Verification of cas no

The CAS Registry Mumber 3114-31-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,1,1 and 4 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 3114-31:
(6*3)+(5*1)+(4*1)+(3*4)+(2*3)+(1*1)=46
46 % 10 = 6
So 3114-31-6 is a valid CAS Registry Number.

3114-31-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(4-Bromo-3-chlorophenyl)ethanone

1.2 Other means of identification

Product number -
Other names 4-bromo-3-chlor-acetophenone

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:3114-31-6 SDS

3114-31-6Relevant academic research and scientific papers

ISOQUINOLINE COMPOUNDS, A PROCESS FOR THEIR PREPARATION, AND PHARMACEUTICAL COMPOSITIONS CONTAINING THEM

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Paragraph 0272; 0273; 0274; 0423; 0424; 0425, (2017/06/12)

A compound of formula (I): wherein the substituents are as defined in the description. Medicinal products containing the same which are useful in treating or preventing pathologies which are the result of activation of the RhoA/ROCK pathway and phosphorylation of the myosin light chain.

DIHYDROPYRIMIDIN-2-ONE COMPOUNDS AND MEDICAL USE THEREOF

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Paragraph 0646-0648, (2016/08/07)

A compound of Formula [I] or a pharmaceutically acceptable salt thereof: wherein each symbol is defined as in the specification.

ACETYLENIC MICROBIOCIDES

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Page/Page column 32-33, (2013/10/21)

Compounds of formula (I), wherein the other substituents HetAr, A', R1, R2, R3, R4, R5, R6, R7, R8 and R9 are as defined in claim 1, and their use in compositions and methods for the control and/or prevention of microbial infection, particularly fungal infection, in plants and to processes for the preparation of these compounds.

Superelectrophilic bromination of deactivated aromatic rings with tribromoisocyanuric acid-an experimental and DFT study

de Almeida, Leonardo S.,Esteves, Pierre M.,de Mattos, Marcio C.S.

experimental part, p. 3001 - 3004 (2009/09/28)

The reaction of deactivated arenes with tribromoisocyanuric acid (TBCA) in 98% H2SO4 produced bromoarenes in good yields. The acidity of the medium controls the strength of the brominating agent and the amount of polybrominated products. DFT calculations at B3LYP/6-311++G** level showed that the protonated TBCA (a superelectrophilic species) can easily transfer Br+ to deactivated arenes, in order to decrease internal charge-charge repulsion.

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