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131136-82-8

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131136-82-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 131136-82-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,1,1,3 and 6 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 131136-82:
(8*1)+(7*3)+(6*1)+(5*1)+(4*3)+(3*6)+(2*8)+(1*2)=88
88 % 10 = 8
So 131136-82-8 is a valid CAS Registry Number.

131136-82-8SDS

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 N,N-Dimethyl-3-methylthiopropanethioamide

1.2 Other means of identification

Product number -
Other names N,N-Dimethyl-3-methylsulfanyl-thiopropionamide

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:131136-82-8 SDS

131136-82-8Downstream Products

131136-82-8Relevant articles and documents

NEW ROUTES TO THIOKETENES AND PROPADIENETHIONE BY FLASH VACUUM THERMOLYSIS.

Vallee, Yannick,Masson, Serge,Ripoll, Jean-Louis

, p. 3921 - 3928 (2007/10/02)

The retro-Diels-Alder reaction under flash vacuum thermolysis (FVT) conditions was applied to the synthesis of simple unstabilized thioketenes.Alternatively, these reactive thiocarbonyl compounds were obtained by FVT elimination of methyltrimethylsilyl sulfide from silylated ketene dithioacetals (and for thioketene itself from methyl trimethylsilyl dithioacetate).A synthesis of propadienethione associationg these two thermolytic processes is also reported.The thermolysis products were identified by low temperature IR spectroscopy and immediate quenching with gaseous dimethylamine leading to the corresponding thioamides.In the case of propadienethione, further reaction with the methanethiol formed in situ was observed.

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