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126496-79-5

126496-79-5

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126496-79-5 Usage

General Description

(S)-tert-butyl methyl aziridine-1,2-dicarboxylate is a chemical compound with the molecular formula C9H15NO4. It is a derivative of aziridine, a three-membered heterocyclic organic compound with a nitrogen atom. The compound is a stable aziridine-1,2-dicarboxylate with a tert-butyl and a methyl group attached to the nitrogen atom. It is commonly used as a reagent in organic synthesis, acting as a source of aziridine nucleophiles. (S)-tert-butyl methyl aziridine-1,2-dicarboxylate has proven to be useful in various reactions, such as the synthesis of amino acids and other complex organic molecules. Additionally, it has potential applications in pharmaceutical research and drug development due to its unique chemical properties.

Check Digit Verification of cas no

The CAS Registry Mumber 126496-79-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,6,4,9 and 6 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 126496-79:
(8*1)+(7*2)+(6*6)+(5*4)+(4*9)+(3*6)+(2*7)+(1*9)=155
155 % 10 = 5
So 126496-79-5 is a valid CAS Registry Number.

126496-79-5SDS

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 (S)-1-tert-Butyl 2-methyl aziridine-1,2-dicarboxylate

1.2 Other means of identification

Product number -
Other names (S)-tert-butyl methyl aziridine-1,2-dicarboxylate

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:126496-79-5 SDS

126496-79-5Relevant articles and documents

A practical method for the aziridination of α,β-unsaturated carbonyl compounds with a simple carbamate utilizing sodium hypochlorite pentahydrate

Minakata, Satoshi,Umeda, Takehiro

, p. 22120 - 22124 (2021/07/02)

The efficient formation oftert-butylN-chloro-N-sodio-carbamate by the reaction of simpletert-butyl carbamate with sodium hypochlorite pentahydrate (NaOCl·5H2O) would be a practical and green method for the aziridination of α,β-unsaturated carbo

Selective cleavage of carbamate protecting groups from aziridines with otera's catalyst

Sun, Shan,Tirotta, Ilaria,Zia, Nicholas,Hutton, Craig A.

, p. 411 - 415 (2014/04/03)

Otera's distannoxane catalyst was found to promote the cleavage of carbamate groups from N-protected aziridines. This method enables the chemoselective cleavage of an aziridinyl N-carbobenzyloxy (Cbz) group in the presence of other N-Cbz groups. The selec

Use of (S)-N-tert-butoxycarbonylaziridine-2-carboxylate derivatives for α-amino acid synthesis

Baldwin, Jack E.,Farthing, Christopher N.,Russell, Andrew T.,Schofield, Christopher J.,Spivey, Alan C.

, p. 3761 - 3764 (2007/10/03)

(S)-tert-Butyl-N-tert-butoxycarbonylaziridine-2-carboxylate and (S)-tert-butyl-N-tert-butoxycarbonylaziridine-2-carboxamide were synthesised and found to react with copper 'catalysed' Grignard reagents to give protected α-amino acids in moderate to good yields.

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