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S-isopropyl-N-p-tolylsulphonylsulphenamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

73853-63-1

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73853-63-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 73853-63-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,8,5 and 3 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 73853-63:
(7*7)+(6*3)+(5*8)+(4*5)+(3*3)+(2*6)+(1*3)=151
151 % 10 = 1
So 73853-63-1 is a valid CAS Registry Number.

73853-63-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name S-isopropyl-N-p-tolylsulphonylsulphenamide

1.2 Other means of identification

Product number -
Other names N-tosyl-2-propanesulfenamide

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:73853-63-1 SDS

73853-63-1Downstream Products

73853-63-1Relevant academic research and scientific papers

Preparation of Alkanesulfenamides by Selective Elimination of t-Butyl Group in S-Alkyl-S-t-butylsulfilimines

Yamamoto, Tamotsu,Kakimoto, Masa-aki,Maejima, Takeshi,Okawara, Makoto

, p. 1249 - 1250 (2007/10/02)

N-Tosylalkanesulfenamides have been prepared via the reaction of alkyl halides with 2-methyl-2-propanethiolate followed by S-imination with chloramine T and the thermolysis.This method comprises the use of selective elimination of t-butyl group in S-alkyl

Selectivity in the Electrophilic Addition of Carbenes and Nitrenes to Aliphatic Sulphides and to 4-t-Butylthian

Appleton, David C.,Bull, David C.,Kenna, James Mc,Kenna, Jean M. Mc,Walley, Andrew R.

, p. 385 - 390 (2007/10/02)

Photogenerated bisalkoxycarbonyl- and diacetyl-carbenes add exclusively equatorially to 4-t-butylthian and exhibit selectivity in competitive additions to mixtures of dimethyl- and di-isopropyl sulphides.By contrast ethoxy-carbonyl- and p-tolylsulphonyl-nitrene give equal proportions of axial and equatorial adducts with the thian, and show no selectivity in competitive reactions with dialkyl sulphides.The results in most or all cases appear to be determined by kinetic control.

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