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o-Xylyl sulphide, also known as 2,3-dimethyl-1,4-benzothiazine, is an organic compound with the chemical formula C8H10S. It is a colorless to pale yellow crystalline solid that is insoluble in water but soluble in organic solvents. o-Xylyl sulphide is derived from the reaction of o-xylene with elemental sulfur, resulting in a sulfur-containing aromatic compound. o-xylyl sulphide is primarily used as an intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals. Due to its unique chemical structure, it exhibits interesting properties such as reactivity towards nucleophiles and electrophiles, making it a valuable building block in organic synthesis.

1215-72-1

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1215-72-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1215-72-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,2,1 and 5 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1215-72:
(6*1)+(5*2)+(4*1)+(3*5)+(2*7)+(1*2)=51
51 % 10 = 1
So 1215-72-1 is a valid CAS Registry Number.

1215-72-1SDS

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 o-xylyl sulphide

1.2 Other means of identification

Product number -
Other names 2,3,2',3'-Tetramethyl-diphenylsulfid

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:1215-72-1 SDS

1215-72-1Relevant academic research and scientific papers

Palladium-Catalyzed Enantioselective C?H Olefination of Diaryl Sulfoxides through Parallel Kinetic Resolution and Desymmetrization

Zhu, Yu-Chao,Li, Yan,Zhang, Bo-Chao,Zhang, Feng-Xu,Yang, Yi-Nuo,Wang, Xi-Sheng

supporting information, p. 5129 - 5133 (2018/03/27)

The first example of PdII-catalyzed enantioselective C?H olefination with non-chiral or racemic sulfoxides as directing groups was developed. A variety of chiral diaryl sulfoxides were synthesized with high enantioselectivity (up to 99 %) throu

Process for the preparation of trichloromethyl-substituted aromatic compounds, and trichloromethyl-substituted aromatic compounds obtained in this process

-

, (2008/06/13)

Trichloromethyl-substituted aromatic compounds are obtained by the chlorination of thioethers of the formula STR1 wherein Ar represents an optionally substituted aryl radial, X1 denotes hydrogen or halogen, and R1 represents optionally substituted alkyl, aralkyl, the nitrile group, an optionally substituted aryl radical or the group STR2 wherein Ar and X have the meaning given. The compounds, of which some are new, can be used as intermediate products for plant protection agents.

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