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35120-10-6

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35120-10-6 Usage

Chemical Properties

clear colourless to yellow liquid

Check Digit Verification of cas no

The CAS Registry Mumber 35120-10-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,5,1,2 and 0 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 35120-10:
(7*3)+(6*5)+(5*1)+(4*2)+(3*0)+(2*1)+(1*0)=66
66 % 10 = 6
So 35120-10-6 is a valid CAS Registry Number.
InChI:InChI=1/C3H5NS/c1-5-3-2-4/h3H2,1H3

35120-10-6 Well-known Company Product Price

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  • Alfa Aesar

  • (L03066)  (Methylthio)acetonitrile, 99%   

  • 35120-10-6

  • 5g

  • 229.0CNY

  • Detail
  • Alfa Aesar

  • (L03066)  (Methylthio)acetonitrile, 99%   

  • 35120-10-6

  • 25g

  • 582.0CNY

  • Detail
  • Alfa Aesar

  • (L03066)  (Methylthio)acetonitrile, 99%   

  • 35120-10-6

  • 100g

  • 2150.0CNY

  • Detail

35120-10-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name (METHYLTHIO)ACETONITRILE

1.2 Other means of identification

Product number -
Other names Acetonitrile, (methylthio)-

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:35120-10-6 SDS

35120-10-6Relevant articles and documents

Synthesis of Unsymmetrical Functionalised Organic Sulphides

Singh, Harjit,Batra, Manohar S.,Singh, Paramjit

, p. 131 - 136 (2007/10/02)

Acyclic thioiminium salts and the condensed thiazolium salts in the presence of aqueous sodium hydroxide as such or under base catalyzed phase transfer catalysis conditions react with appropiate organic halides to provide corresponding unsymmetrical functionalized organic sulphides.With aqueous sodium hydroxide, thioiminium salts provide the disulphides corresponding to incipient thiol.

Synthesis of Functionalised, Unsymmetrical Organic Sulphides - Thioacetamide as a Sulphur Transfer Reagent

Singh, Harjit,Malhotra, Nageshwar,Batra, Manohar S.

, p. 272 - 273 (2007/10/02)

In a novel approach, unsymmetrical organic sulphides (IIa-h) have been obtained from appropriate organic halides and sulphonium salts (I) - a source of incipient thiolate ions.

Thio and sulfonyl glyoxylnitrileoxime phosphates and phosphonates

-

, (2008/06/13)

Compounds of the formula EQU1 in which R is lower alkyl; R1 is lower alkyl or lower alkoxy; X is thio or sulfonyl; R2 is alkyl, benzothiazolo, benzyl, naphthyl, benzodiazolo-1,3, thiazolo, phenyl or substituted phenyl wherein said substituents are chloro, bromo, methyl or methoxy and the use of these compounds as insecticides.

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