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57663-14-6

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57663-14-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 57663-14-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,7,6,6 and 3 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 57663-14:
(7*5)+(6*7)+(5*6)+(4*6)+(3*3)+(2*1)+(1*4)=146
146 % 10 = 6
So 57663-14-6 is a valid CAS Registry Number.

57663-14-6SDS

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 2,6,6-trimethyl-1-phenyl-5,7-dihydroindol-4-one

1.2 Other means of identification

Product number -
Other names 1-phenyl-2,6,6-trimethyl-4,5,6,7-tetrahydroindol-4-one

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:57663-14-6 SDS

57663-14-6Relevant articles and documents

Synthesis, molecular docking, and in silico ADME/Tox profiling studies of new 1-aryl-5-(3-azidopropyl)indol-4-ones: Potential inhibitors of SARS CoV-2 main protease

Domínguez-Villa, Francisco Xavier,Durán-Iturbide, Noemi Angeles,ávila-Zárraga, José Gustavo

supporting information, (2020/12/07)

The virus SARS CoV-2, which causes the respiratory infection COVID-19, continues its spread across the world and to date has caused more than a million deaths. Although COVID-19 vaccine development appears to be progressing rapidly, scientists continue th

Tetrahydropyrrolo[3,2-c]azepin-4-ones as a new class of cytotoxic compounds

Martínez, Roberto,ávila, J. Gustavo,Ramírez, Ma. Teresa,Pérez, Araceli,Martínez, ángeles

, p. 4007 - 4016 (2007/10/03)

Pyrroloazepinones 8a-j and 9a-j were designed by structural modification of lead compound 3. These compounds were tested on five tumor cell lines to determine the role of the azeto ring and the 2-methyl substituent in the cytotoxicity of compound 3. Our r

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