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428868-52-4

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428868-52-4 Usage

Uses

Fmoc-nalpha-methyl-o-benzyl-l-tyrosine

Check Digit Verification of cas no

The CAS Registry Mumber 428868-52-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,2,8,8,6 and 8 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 428868-52:
(8*4)+(7*2)+(6*8)+(5*8)+(4*6)+(3*8)+(2*5)+(1*2)=194
194 % 10 = 4
So 428868-52-4 is a valid CAS Registry Number.

428868-52-4SDS

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-Nalpha-methyl-O-benzyl-L-tyrosine

1.2 Other means of identification

Product number -
Other names N-(carbomethoxy)-3-ethyl-1,2,5,6-tetrahydropyridine

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:428868-52-4 SDS

428868-52-4Downstream Products

428868-52-4Relevant academic research and scientific papers

N-METHYL AMINO ACIDS

-

Page 33; 39, (2010/02/06)

The present invention relates to a compound of formula (I) or (II), processes for preparing them, peptides including them and kits involving them.

An efficient synthesis of N-methyl amino acids by way of intermediate 5-oxazolidinones

Aurelio, Luigi,Box, John S.,Brownlee, Robert T. C.,Hughes, Andrew B.,Sleebs, Marianne M.

, p. 2652 - 2667 (2007/10/03)

N-Methyl amino acids occur in many natural products. Experimental strategies are presented for a unified approach to the synthesis of N-methyl derivatives through 5-oxazolidinones of the 20 common L-amino acids. The amino acids with reactive side chains that required protecting groups or devoted syntheses for side chain construction for N-methylation to proceed included serine, threonine, tyrosine, cysteine, methionine, tryptophan, asparagine, histidine, and arginine. The studies have provided improved methods for the preparation of N-methyl serine, threonine, and tyrosine. All 20 of the common L-amino acids are now available in suitable forms for solid or solution-phase peptide synthesis.

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