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Aziridine, 1-[(2,4-dinitrophenyl)thio]-2-methyl-3-phenyl-, trans- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

73155-20-1

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73155-20-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 73155-20-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,1,5 and 5 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 73155-20:
(7*7)+(6*3)+(5*1)+(4*5)+(3*5)+(2*2)+(1*0)=111
111 % 10 = 1
So 73155-20-1 is a valid CAS Registry Number.

73155-20-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (2S,3S)-1-(2,4-dinitrophenyl)sulfanyl-2-methyl-3-phenylaziridine

1.2 Other means of identification

Product number -
Other names Aziridine,1-[(2,4-dinitrophenyl)thio]-2-methyl-3-phenyl-,trans

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:73155-20-1 SDS

73155-20-1Relevant academic research and scientific papers

Moderate generation of sulfenylnitrenes from novel N-sulfenylsulfodiimides

Yoshimura, Toshiaki,Fujie, Tetsuo,Fujii, Takayoshi

, p. 427 - 430 (2008/02/04)

N-Sulfenylated sulfodiimides were first prepared by the reaction of S,S-diphenyl-N-tosylsulfodiimide with arenesulfenyl chlorides under the basic conditions. Thermolysis of S,S-diphenyl-N-(2-nitrophenylsulfenyl)- and S,S-diphenyl-N-(2,4-dinitrophenylsulfe

An Efficient Thermal Route to Arenesulphenylnitrenes

Atkinson, Robert S.,Lee, Michael,Malpass, John R.

, p. 919 - 920 (2007/10/02)

Arenesulphenylnitrenes are generated efficiently from sulphenamides, (1), on heating at ca. 80 - 120 deg C and are trapped by alkenes as the corresponding aziridines in quantitative yield; this approach is shown to be more efficient and more widely applic

2,4-Dinitrobenzenesulphenylnitrene: Addition to (Z)- and (E)-1-Phenylpropene

Atkinson, Robert S.,Judkins, Brian D.,Khan, Naeema

, p. 2491 - 2498 (2007/10/02)

Oxidation of 2,4-dinitrobenzenesulphenamide (1) with lead tetra-acetate in the presence of (Z)-1-phenylpropene gives a ca. 3:1 mixture of cis- and trans-aziridines (3) and (4), respectively.This ratio is unchanged over a ten-fold decrease in concentration

Intermolecular Trapping of Sulphenylnitrenes by Alkenes

Atkinson, Robert S.,Judkins, Brian D.

, p. 2615 - 2619 (2007/10/02)

Oxidation of 2,4-dinitrobenzenesulphenamide with lead tetra-acetate in the presence of electron-rich alkenes (styrene, (E)- and (Z)-1-phenylpropene, 2-phenylpropene, (Z)-but-2-ene, and butadiene) gives the corresponding substituted N-(2,4-dinitrophenylsulphenyl))aziridines.Intermolecular trapping of a presumed sulphenylnitrene intermediate is also successful in the oxidation of 2-nitrobenzenesulphenamide but fails for RSNH2 when R = PhCO, 4-ClC6H4, or 4-NO2C6H4.

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