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Hydrazinecarboxylic acid, 2-(3-amino-3-oxopropyl)-, 1,1-dimethylethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

133382-89-5

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133382-89-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 133382-89-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,3,3,8 and 2 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 133382-89:
(8*1)+(7*3)+(6*3)+(5*3)+(4*8)+(3*2)+(2*8)+(1*9)=125
125 % 10 = 5
So 133382-89-5 is a valid CAS Registry Number.

133382-89-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name tert-butyl N-[(3-amino-3-oxopropyl)amino]carbamate

1.2 Other means of identification

Product number -
Other names 3-(N'-tert-butoxycarbonylhydrazino)propanamide

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:133382-89-5 SDS

133382-89-5Relevant academic research and scientific papers

Preparation of new monomers aza-β3-aminoacids for solid-phase syntheses of aza-β3-peptides

Busnel, Olivier,Baudy-Floc'h, Miche?le

, p. 5767 - 5770 (2008/02/09)

The preparation of new Nβ-Fmoc-protected aza-β3-amino acids (aza-β3-aa) with proteinogenic side chains as well as their Nβ-Fmoc, Nβ-Cbz or Nβ-Boc aza-β3-amino esters (from Pro, Asn, Asp, Glu, Gln) by successive nucleophilic substitutions will be described.

Synthesis and spectroscopic properties of azaglutamine amino acid and peptide derivatives

Gray,Quibell,Jiang,Baggett

, p. 141 - 146 (2007/10/02)

tert-Butyl carbazate and Boc-amino acid hydrazides undergo a Michael addition with acrylamide to give substituted carbazates having the side-chain of glutamine on nitrogen. These carbazates may react with chloroformates to give protected azaglutamine esters, and N-activated amino acid esters to give azaglutamine peptides.

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