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41374-14-5

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41374-14-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 41374-14-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,1,3,7 and 4 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 41374-14:
(7*4)+(6*1)+(5*3)+(4*7)+(3*4)+(2*1)+(1*4)=95
95 % 10 = 5
So 41374-14-5 is a valid CAS Registry Number.

41374-14-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,2-bis(methylsulfanyl)ethenylsulfonylbenzene

1.2 Other means of identification

Product number -
Other names 1,1-Di-methylthio-2-(phenylsulfonyl)-ethen

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:41374-14-5 SDS

41374-14-5Relevant articles and documents

Synthesis of pharmaceutically important heteroaromatics from methyl phenyl sulfone

Yokoyama,Tsuji,Imamoto

, p. 2954 - 2956 (1984)

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Imidazolylalkylthioalkylamino-ethylene derivatives

-

, (2008/06/13)

Compounds of the formula STR1 wherein R1 is a straight or branched chain alkynyl group containing from 3 to 9 carbon atoms, inclusive; R2 is hydrogen, (lower)alkyl, halogen or hydroxymethyl; m is 1 or 2, and n is 2 or 3, provided that the sum of m and n is 3 or 4; X and Y each are independently hydrogen, nitro, cyano, --SO2 Ar or --COR3, provided that X and Y are not both hydrogen; R3 is (lower)alkyl, Ar, (lower)alkoxy, amino or (lower)-alkylamino; and Ar is an optionally substituted phenyl group; and nontoxic pharmaceutically acceptable acid addition salts thereof, are potent anti-ulcer agents. Processes for their preparation and novel intermediates are also disclosed.

IMIDAZOLE ALKYLAMINOETHYLENE COMPOUNDS

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, (2008/06/13)

The compounds are ethylene derivatives which are inhibitors of histamine activity, in particular, inhibitors of H-2 histamine receptors. A compound of this invention is 1-nitro-2-methylamino-2-2-((4-methyl-5-imidazolyl)methylthio)-ethylamino!ethylene.

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