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4-(2-bromopropanoyl)phenyl benzoate is a chemical compound with the molecular formula C16H13BrO3. It is an organic ester derived from benzoic acid and 4-(2-bromopropanoyl)phenol. 4-(2-bromopropanoyl)phenyl benzoate is characterized by the presence of a bromine atom attached to a propane chain, which is connected to a phenyl ring through an ester linkage. The structure of 4-(2-bromopropanoyl)phenyl benzoate features a benzene ring (C6H5) attached to a benzoate group (C7H5O2), with the bromine-substituted propane chain extending from the para position of the phenyl ring. 4-(2-bromopropanoyl)phenyl benzoate may have potential applications in the synthesis of pharmaceuticals, agrochemicals, or other specialty chemicals due to its unique structure and reactivity.

35282-40-7

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35282-40-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 35282-40-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,5,2,8 and 2 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 35282-40:
(7*3)+(6*5)+(5*2)+(4*8)+(3*2)+(2*4)+(1*0)=107
107 % 10 = 7
So 35282-40-7 is a valid CAS Registry Number.

35282-40-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name [4-(2-bromopropanoyl)phenyl] benzoate

1.2 Other means of identification

Product number -
Other names -

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

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More Details:35282-40-7 SDS

35282-40-7Relevant academic research and scientific papers

PROCESS FOR PRODUCING OPTICALLY ACTIVE s-AMINO ALCOHOL

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Page/Page column 29, (2008/06/13)

A process for easily producing an optically active β-amino alcohol useful as a pharmaceutical intermediate from an inexpensive, readily available starting material is provided. A readily available α-substituted ketone is reacted with an optically active amine to yield a diastereomer mixture of an optically active α-substituted aminoketone. One of the diastereomers is isolated optionally after the diastereomers are converted to salts with an acid. The optically active α-substituted aminoketone or a salt thereof thus isolated was stereoselectively reduced to yield an optically active β-substituted amino alcohol. The optically active β-substituted amino alcohol is subjected to hydrogenolysis to produce an optically active β-amino alcohol or a salt thereof.

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