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6H-1,3-Thiazine-6-thione, 2-(methylthio)-4-phenyl-5-(phenylsulfonyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

93202-11-0

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93202-11-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 93202-11-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,3,2,0 and 2 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 93202-11:
(7*9)+(6*3)+(5*2)+(4*0)+(3*2)+(2*1)+(1*1)=100
100 % 10 = 0
So 93202-11-0 is a valid CAS Registry Number.

93202-11-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-methylthio-4-phenyl-5-phenylsulfonyl-1,3-thiazine-6(6H)-thione

1.2 Other means of identification

Product number -
Other names 2-methylthio-4-phenyl-5-phenylsulfonyl-1,3-thiazine-6-thione

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:93202-11-0 SDS

93202-11-0Relevant academic research and scientific papers

Reactions of 1,3-thiazine-2,6-dithiones. part 8.1 formation of a new series of 2-pyrroline-4-thiones by the rearrangement of 1,3-thiazine-6-spiro-2’-thiirane-2-thiones and 2-methylthio-1,3(6h)-thiazine-6-spiro-2’-thiiranes and some related reactions

Yamamoto, Tatsuo,Miyamae, Hiroshi,Muraoka, Motomu

, p. 641 - 663 (2018/04/23)

1,3(6H)-Thiazine-6-spiro-2’-thiirane-2-thiones 2a-c and 3’,3’-disubstituted 2-methylthio-1,3-thiazine-6-spiro-2’-thiiranes 12a-f were synthesized by the reaction of 1,3-thiazine-2,6-dithiones 1 or 11a-d, which are 2-methylthio derivatives of thiazinedithiones 1, with diazomethane derivatives. 1,3(6H)-Thiazine-6-spiro-2’-thiiranes 2a-c and 12a-f rearranged into a series of 2-pyrroline-4-thione derivatives 3a-c and methyl 4-thioxopyrroline-1-dithiocarboxylates 13a-f on treatment with a base or gentle heating. 2-Pyrroline-4-thione derivative 13c, upon heating to 140 oC for 1 h, reversely rearranged into the thiirane derivative 12c. The structure of the 2-pyrroline-4-thione 13e was determined by single-crystal X-ray analysis.

Reactions of 1,3-Thiazine-2,6-dithiones. Part 7. Formation Reactions of 3-Thioureidocinnamthioamides, 3-- and 3-dithiocinnamic Acid Esters by the Thiazine Ring Opening Reactions with primary Amines,

Yamamoto, Tatsuo,Muraoka, Motomu

, p. 835 - 846 (2007/10/02)

2-Alkylamino- and 2-arylamino-1,3-thiazine-6-thiones 3 were synthesized by the reactions of 1,3-thiazine-2,6-dithiones 1 or 2-methylthio-1,3-thiazine-6-thiones 2 with aliphatic or aromatic primary amines. 3-(3-Alkylthioureido)cinnamthioamides 4 were forme

Reactions of 1,3-Thiazine-2,6-dithiones. Part 6 . Synthesis of 2-Alkylthio-2,3-dihydro-1,3-thiazine-6-thiones by Reductive Alkylation of 1,3-Thiazine-2,6-dithiones

Muraoka, Motomu,Yamada, Atsushi,Yamamoto, Tatsuo

, p. 953 - 955 (2007/10/02)

2-Alkylthio-2,3-dihydro-1,3-thiazine-6-thiones 4 are synthesized by the reductive alkylation of 1,3-thiazine-2,6-dithiones with thiolate anions.

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