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Aziridine, 2,3-diethyl-1-[(4-methylphenyl)sulfonyl]-, (2R,3S)-rel- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

328584-49-2

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328584-49-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 328584-49-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,2,8,5,8 and 4 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 328584-49:
(8*3)+(7*2)+(6*8)+(5*5)+(4*8)+(3*4)+(2*4)+(1*9)=172
172 % 10 = 2
So 328584-49-2 is a valid CAS Registry Number.

328584-49-2SDS

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 2,3-diethyl-1-[(4-methylphenyl)sulfonyl]aziridine

1.2 Other means of identification

Product number -
Other names (2S,3R)-2,3-Diethyl-1-(toluene-4-sulfonyl)-aziridine

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:328584-49-2 SDS

328584-49-2Downstream Products

328584-49-2Relevant academic research and scientific papers

Copper(ii) complexes incorporating poly/perfluorinated alkoxyaluminate-type weakly coordinating anions: Syntheses, characterization and catalytic application in stereoselective olefin aziridination

Li, Yang,He, Jiayue,Khankhoje, Vineeta,Herdtweck, Eberhardt,Koehler, Klaus,Storcheva, Oksana,Cokoja, Mirza,Kuehn, Fritz E.

supporting information; experimental part, p. 5746 - 5754 (2011/08/02)

The synthesis and characterization of a series of cationic copper(ii) complexes of the type [Cu(NCR)6][Al(OC(CF3) 2R′)4]2 (R = CH3, Ph; R′ = CF3, Ph, PhCH3), incorpora

A facile noncatalytic pathway for the nitrene transfer process: Expeditious access to aziridines

Saikia, Indranirekha,Kashyap, Bishwapran,Phukan, Prodeep

, p. 2967 - 2969 (2011/04/24)

A fast and efficient method has been developed for generation of sulfonyl nitrene from N,N-dibromo-p-toluenesulfonamide (TsNBr2) in the presence of a base without any catalyst. This method was applied to produce aziridines from different kinds of olefins within a short time in high yields. The Royal Society of Chemistry.

Regio- and stereospecific synthesis of β-sulfonamidodisulfides and β-sulfonamidosulfides from aziridines using tetrathiomolybdate as a sulfur transfer reagent

Sureshkumar, Devarajulu,Gunasundari, Thanikachalam,Ganesh, Venkataraman,Chandrasekaran, Srinivasan

, p. 2106 - 2117 (2007/10/03)

A comprehensive study of a general and effective one-step procedure for the synthesis of β-sulfonamidodisulfides directly from N-tosyl aziridines in a regio- and stereospecific manner under neutral conditions without the use of any Lewis acid or base has been reported. This methodology is extended to the synthesis of an optically pure cyclic seven-membered disulfide 29. Synthesis of a variety of β-sulfonamidosulfides involving tandem, multistep reactions in one pot is also reported.

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