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FMOC-BETA-N-BENZYLAMINO-D-ALA is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1217633-31-2

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1217633-31-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1217633-31-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,1,7,6,3 and 3 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1217633-31:
(9*1)+(8*2)+(7*1)+(6*7)+(5*6)+(4*3)+(3*3)+(2*3)+(1*1)=132
132 % 10 = 2
So 1217633-31-2 is a valid CAS Registry Number.

1217633-31-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (R)-2-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)-3-(benzylamino)propanoic acid

1.2 Other means of identification

Product number -
Other names -

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:1217633-31-2 SDS

1217633-31-2Upstream product

1217633-31-2Downstream Products

1217633-31-2Relevant academic research and scientific papers

Synthetic strategy for side chain mono-N-alkylation of Fmoc-amino acids promoted by molecular sieves

Monfregola, Luca,De Luca, Stefania

, p. 981 - 990 (2011)

A new synthetic strategy to alkylate amino groups under mild conditions has been developed. It utilizes only 4 A molecular sieves as base in order to promote the N-alkylation reaction, in presence of the appropriate alkyl halide. The methodology was validated by the simple and efficient side-chain N-alkylation of o-Ns-protected Fmoc-amino acid. One of them was introduced as building block into a peptide sequence, thus allowing the preparation of site-specific alkylated peptide molecules. Springer-Verlag 2010.

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