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5202-11-9

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5202-11-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5202-11-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,2,0 and 2 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 5202-11:
(6*5)+(5*2)+(4*0)+(3*2)+(2*1)+(1*1)=49
49 % 10 = 9
So 5202-11-9 is a valid CAS Registry Number.

5202-11-9SDS

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 2-methyldibenzo[b,e]thiepin-11(6H)-one

1.2 Other means of identification

Product number -
Other names 2-methyl-6H-dibenzo[b,e]thiepin-11-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:5202-11-9 SDS

5202-11-9Relevant articles and documents

Synthesis of benzyl sulfidesviasubstitution reaction at the sulfur of phosphinic acid thioesters

Nishiyama, Yoshitake,Hosoya, Takamitsu,Yoshida, Suguru

supporting information, p. 5771 - 5774 (2020/06/03)

An ambident electrophilicity of phosphinic acid thioesters is disclosed. Unexpected carbon-sulfur bond formation took place in the reaction between phosphinic acid thioesters and benzyl Grignard reagents. The developed method for benzyl sulfides has a wide substrate scope and was applicable for the synthesis of a drug analog.

Acid-Catalyzed Reactions of Ortho-Substituted Benzohydroxamic Acids in Polyphosphoric Acid (PPA)

Chhaya, P. N.,Nimbalkar, M. M.,Hosangadi, B. D.

, p. 4458 - 4460 (2007/10/02)

Ortho-substituted benzohydroxamic acids undergo a variety of reactions when treated with PPA.The nature of substituents on the ring and on the functional group CONHOH plays a key role in influencing the reaction pathways.The difference in behavior may arise due to change in site of protonation depending upon the substitution.However, no clear-cut relationship could be established as attempts to monitor reactions on NMR proved inconclusive.

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