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1H-Indole, 2-acetyl-3-methyl-1-(phenylsulfonyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

143774-63-4

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143774-63-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 143774-63-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,3,7,7 and 4 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 143774-63:
(8*1)+(7*4)+(6*3)+(5*7)+(4*7)+(3*4)+(2*6)+(1*3)=144
144 % 10 = 4
So 143774-63-4 is a valid CAS Registry Number.

143774-63-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-[1-(benzenesulfonyl)-3-methylindol-2-yl]ethanone

1.2 Other means of identification

Product number -
Other names 2-acetyl-3-methyl-N-benzenesulfonylindole

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:143774-63-4 SDS

143774-63-4Relevant academic research and scientific papers

Cyclocondensation reactions between 2-acyl-3-indoleacetic acid derivatives and phenylglycinol: Enantioselective synthesis of 1-substituted tetrahydro-β-carboline alkaloids

Amat, Mercedes,Subrizi, Fabiana,Elias, Viviane,Llor, Nuria,Molins, Elies,Bosch, Joan

, p. 1835 - 1842 (2012/05/05)

Cyclocondensation reactions between a variety of 2-acyl-3-indoleacetic acid derivatives and (R)-phenylglycinol were studied. Successful results were obtained from N-alkyl keto acid derivatives. The resulting tetracyclic lactams provide straightforward access to enantiopure 1-substituted tetrahydro-β- carboline alkaloids.

A direct lithiation route to 2-acyl-1-(phenylsulfonyl)indoles

Jiang, Jun,Gribble, Gordon W.

, p. 2035 - 2040 (2007/10/03)

2-Acyl-1-(phenylsulfonyl)indoles (3, 7-9) are prepared in 75-84% yield from 1-(phenylsulfonyl)indoles (1, 5) in one operation by treatment of the latter with s-butyllithium followed by inverse quenching of the C-2 lithioindoles with carboxylic acid anhydr

Synthesis of 1-keto-3-thia-1,2,3,4-tetrahydrocarbazole ring system

Mohanakrishnan, A. K.,Srinivasan, P. C.

, p. 838 - 841 (2007/10/03)

Synthesis of 1-keto-3-thia-1,2,3,4-tetrahydrocarbazole ring system and some of its reactions leading to the formation of aldol (8), sulfoxide (10) and sulfone (11) are reported.

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