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1,4,2,3-Dithiadiazine, 5,5,6,6-tetrachlorotetrahydro-2,3-bis(4-methylphenyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

137838-63-2

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137838-63-2 Usage

Structure

Tetrachlorinated derivative of tetrahydrodithiadiazine

Substituents

Contains two 4-methylphenyl groups attached to the nitrogen atoms

Family

Dithiadiazine family

Potential applications

Pesticides and pharmaceuticals

Availability of properties and uses

Not readily available, but structure suggests potential as a pesticide or pharmaceutical compound

Check Digit Verification of cas no

The CAS Registry Mumber 137838-63-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,7,8,3 and 8 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 137838-63:
(8*1)+(7*3)+(6*7)+(5*8)+(4*3)+(3*8)+(2*6)+(1*3)=162
162 % 10 = 2
So 137838-63-2 is a valid CAS Registry Number.

137838-63-2SDS

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 2,3-bis(4-methylphenyl)-5,5,6,6-tetrachloro-2,3,5,6-tetrahydro-1,4,2,3-dithiadiazine

1.2 Other means of identification

Product number -
Other names 5,5,6,6-Tetrachloro-2,3-di-p-tolyl-[1,4,2,3]dithiadiazinane

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:137838-63-2 SDS

137838-63-2Downstream Products

137838-63-2Relevant academic research and scientific papers

Generation and selected reactions of chlorinated thiocarbonyl S-imides*

Mlostoń, Grzegorz,Pipiak, Paulina,Voss, Jürgen,Buddensiek, Dirk,Senning, Alexander

, p. 530 - 547 (2017/09/27)

N-Aryl-1,1,1-trichloromethanesulfenamides ArNH-SCCl3 easily undergo dehydrochlorination upon treatment with potassium hydroxide in ethanolic solution. The intermediate thiocarbonyl S-imides formed thereby behave differently depending on the typ

Formation of a 1,4,2,3-Dithiadiazine via Dimerization of a Transient Thione-S-imide (Thiocarbonyl Imine Dipole)

Potts, Kevin T,,Baum, Jonathan S.

, p. 1637 - 1640 (2007/10/02)

N-(p-Tolyl)trichloromethane sulfenamide when treated with potassium hydroxide in an ether-alcohol mixture resulted in the formation in solution of a red, transient thione-S-imide which underwent a head-to-head dimerization to 2,3-di(p-tolyl)-5,5,6,6-tetra

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