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Glycine, N-[N-[(1,1-dimethylethoxy)carbonyl]-D-alanyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

66444-38-0

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66444-38-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 66444-38-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,6,4,4 and 4 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 66444-38:
(7*6)+(6*6)+(5*4)+(4*4)+(3*4)+(2*3)+(1*8)=140
140 % 10 = 0
So 66444-38-0 is a valid CAS Registry Number.

66444-38-0SDS

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 2-[[(2R)-2-[(2-methylpropan-2-yl)oxycarbonylamino]propanoyl]amino]acetic acid

1.2 Other means of identification

Product number -
Other names Glycine,N-[N-[(1,1-dimethylethoxy)carbonyl]-D-alanyl]

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:66444-38-0 SDS

66444-38-0Upstream product

66444-38-0Relevant academic research and scientific papers

Synthesis and properties of N(α)-(tert-butyloxycarbonyl)peptide p- guanidinophenyl esters as trypsin substrates

Itoh,Sekizaki,Toyota,Tanizawa

, p. 2082 - 2087 (2007/10/03)

N(α)-(tert-Butyloxycarbonyl)peptide p-guanidinophenyl esters were synthesized by amidination of N(α)-(tert-butyloxycarbonyl)peptide p- aminophenyl esters with 1-[N,N'-bis(benzyloxycarbonyl)amidino]pyrazole, followed by deprotection by catalytic hydrogenation, in good total yields. These synthetic esters were characterized as specific substrates for trypsin, and kinetic parameters for the trypsin-catalyzed hydrolysis are presented.

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