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92013-30-4

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92013-30-4 Usage

General Description

4-(2-Bromophenyl)butanoyl chloride is a chemical compound with the formula C10H10BrClO. It is a derivative of butanoyl chloride, with a bromophenyl group attached at the 4-position. 4-(2-BROMOPHENYL)BUTANOYL CHLORIDE is commonly used in organic synthesis as a versatile intermediate for the production of various pharmaceuticals and agrochemicals. It is a reactive compound that is sensitive to moisture and air, and should be handled with caution in a controlled laboratory environment.

Check Digit Verification of cas no

The CAS Registry Mumber 92013-30-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,2,0,1 and 3 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 92013-30:
(7*9)+(6*2)+(5*0)+(4*1)+(3*3)+(2*3)+(1*0)=94
94 % 10 = 4
So 92013-30-4 is a valid CAS Registry Number.

92013-30-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(2-bromophenyl)butanoyl chloride

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

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

More Details:92013-30-4 SDS

92013-30-4Relevant articles and documents

Novel ligands for the human histamine H1 receptor: Synthesis, pharmacology, and comparative molecular field analysis studies of 2-dimethylamino-5-(6)-phenyl-1,2,3,4-tetrahydronaphthalenes

Ghoneim, Ola M.,Legere, Jacqueline A.,Golbraikh, Alexander,Tropsha, Alexander,Booth, Raymond G.

, p. 6640 - 6658 (2007/10/03)

This paper reports the synthesis of a novel series of (±)-2-dimethylamino- 5- and 6-phenyl-1,2,3,4-tetrahydronaphthalene derivatives (5- and 6-APTs), and, corresponding affinity, functional activity, and, molecular modeling studies with regard to drug des

Synthesis of Biological Markers in Fossil Fuels. 2. Synthesis and 13C NMR Studies of Substituted Indans and Tetralins

Adamczyk, Maciej,Watt, David S.,Netzel, Daniel A.

, p. 4226 - 4237 (2007/10/02)

Unambiguous syntheses of all possible methyl, ethyl, n-propyl, and n-butyl derivatives of indan and tetralin were developed using the Kumada coupling procedure involving the reaction of aryl or vinyl halides with Grignard reagents in the presence of nickel(II) chloride.An analysis of the 13C NMR spectra of these compounds was also completed.

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