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77507-53-0

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77507-53-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 77507-53-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,7,5,0 and 7 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 77507-53:
(7*7)+(6*7)+(5*5)+(4*0)+(3*7)+(2*5)+(1*3)=150
150 % 10 = 0
So 77507-53-0 is a valid CAS Registry Number.

77507-53-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name (1-phenylsulfonyl-3-methyl-1H-indol-2-yl)(phenyl)methanone

1.2 Other means of identification

Product number -
Other names 2-benzoyl-3-methyl-1-(phenylsulfonyl)indole

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:77507-53-0 SDS

77507-53-0Relevant articles and documents

Construction of pyrrole- and indole-fused CF3-piperazine derivatives

Tian, Yu-Ting,Zong, Yu-Wei,Nie, Jing,Zhang, Fa-Guang,Ma, Jun-An

, (2019/09/03)

A series of pyrrole- and indole-fused trifluoromethyl-functionalized piperazine derivatives were constructed in moderate to good yields with excellent chemoselectivities via a Pictet-Spengler reaction under mild and operationally simple conditions. The synthetic utility of this protocol was further extended by the facile preparation of indole-fused CF3-1,4-diazocane and enantioenriched CF3-piperazines via a vinylogous Pictet-Spengler reaction and an asymmetric Pictet-Spengler reaction, respectively.

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

A New Synthesis of the Antitumor 6H-Pyridocarbazole Alkaloid Ellipticine

Kano, Shinzo,Sugino, Eiichi,Shibuya, Shiroshi,Hibino, Satoshi

, p. 2979 - 2981 (2007/10/02)

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