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2-[(3-methylbenzoyl)amino]-N-propyl-4,5,6,7-tetrahydro-1-benzothiophene-3-carboxamide is a complex organic compound with a molecular formula of C19H24N2O2S. It is a derivative of benzothiophene, a heterocyclic compound consisting of a benzene ring fused to a thiophene ring. The molecule features a 3-methylbenzoyl group attached to an amino group, which is further connected to a propyl chain. The compound also contains a carboxyamide group at the 3-position of the benzothiophene ring. This chemical is known for its potential applications in pharmaceuticals and as a chemical intermediate in the synthesis of various compounds. Its structure and properties make it a versatile building block in organic chemistry, particularly in the development of new drugs and other specialty chemicals.

5837-47-8

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5837-47-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5837-47-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,8,3 and 7 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 5837-47:
(6*5)+(5*8)+(4*3)+(3*7)+(2*4)+(1*7)=118
118 % 10 = 8
So 5837-47-8 is a valid CAS Registry Number.

5837-47-8SDS

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-[(3-methylbenzoyl)amino]-N-propyl-4,5,6,7-tetrahydro-1-benzothiophene-3-carboxamide

1.2 Other means of identification

Product number -
Other names dimethallyl ketone

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:5837-47-8 SDS

5837-47-8Downstream Products

5837-47-8Relevant academic research and scientific papers

α-Amino Acids as Nucleophilic Acyl Equivalents, IV. Synthesis of Symmetrical Ketones by Means of 2-Phenyl-2-oxazolin-5-one

Lohmar, Rainald,Steglich, Wolfgang

, p. 3706 - 3715 (2007/10/02)

2-Phenyl-2-oxazolin-5-one (2), itself easily derivable from hippuric acid (1), on reaction with allyl, benzyl or phenacyl halides undergoes 4,4-disubstitution, if the reaction is conducted in dipolar aprotic solvents in presence of weak bases.Hydrolysis of the resulting oxazolinones 3 leads to α,α-dialkylaed hippuric acids 4, which may be oxidized to symmetrical ketones 5 by means of lead tetraacetate.

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