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4-Bromo-2-phenyl-butyric acid is a chemical compound with the molecular formula C10H11BrO2. It is a white crystalline solid that is soluble in organic solvents such as ethanol and acetone. 4-BROMO-2-PHENYL-BUTYRIC ACID is primarily used as an intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals. It is also known for its potential applications in the development of new drugs and as a building block in the creation of complex organic molecules. The compound's structure features a butyric acid chain with a bromine atom at the 4-position and a phenyl group at the 2-position, which contributes to its reactivity and utility in chemical synthesis.

6836-99-3

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6836-99-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6836-99-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,8,3 and 6 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 6836-99:
(6*6)+(5*8)+(4*3)+(3*6)+(2*9)+(1*9)=133
133 % 10 = 3
So 6836-99-3 is a valid CAS Registry Number.
InChI:InChI=1/C10H11BrO2/c11-7-6-9(10(12)13)8-4-2-1-3-5-8/h1-5,9H,6-7H2,(H,12,13)

6836-99-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-bromo-2-phenylbutanoic acid

1.2 Other means of identification

Product number -
Other names 4-bromo-2-phenylbutyric acid

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 -
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More Details:6836-99-3 SDS

6836-99-3Relevant academic research and scientific papers

PREPARATION OF ALPHA-ARYL GAMMA-BUTYROLACTONES

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, (2008/06/13)

This appliciation discloses a process for preparing a lactone of general formula (I), where R is an optionally substituted phenyl group or an optionally substituted mono-or bicyclic heteroaryl radical which process comprises reacting an anion of a malonate of formula (II) with an ethylene compound of formula (III) Y--CH 2--CH 2 OZ, to give a compound of formula (IV) and hydrolysing the compound of formula (IV) to give a lactone of formula (I). The lactones are of use as intermediates for preparing 5-HT 1A binding agents. STR1

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