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FMoc-N-Me-beta-Ala-OH is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

172965-84-3

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172965-84-3 Usage

Uses

Fmoc-beta-MeAla-OH

Check Digit Verification of cas no

The CAS Registry Mumber 172965-84-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,2,9,6 and 5 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 172965-84:
(8*1)+(7*7)+(6*2)+(5*9)+(4*6)+(3*5)+(2*8)+(1*4)=173
173 % 10 = 3
So 172965-84-3 is a valid CAS Registry Number.

172965-84-3SDS

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 Fmoc-N-methyl-β-alanine

1.2 Other means of identification

Product number -
Other names Fmoc-Nle-OPfp

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:172965-84-3 SDS

172965-84-3Downstream Products

172965-84-3Relevant academic research and scientific papers

'One-pot' methylation of Fmoc amino acids

Luke, Richard W. A.,Boyce, Patrick G. T.,Dorling, E. Kate

, p. 263 - 266 (1996)

We report here a convenient method for the conversion of Fmoc amino acids to their N-methylated derivatives. The method involves reaction with formaldehyde and then reduction with triethylsilane (TES). The method is particularly attractive in that the alkylation and reduction are carried out in situ and the reaction sequence and purification of product can readily be carried out in one day. A further advantage is that the method is not restricted to α-amino acids.

Constrained β-alanine based GpIIb/IIIa antagonists

Klein, Scott I.,Czekaj, Mark,Molino, Bruce F.,Valeria, Chu

, p. 1773 - 1778 (2007/10/03)

The concepts of centrally constrained and peptide based fibrinogen receptor antagonists have been successfully combined into a single series of analogs which have been demonstrated to be potent inhibitors of platelet aggregation.

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