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L-Serine, N-(trifluoroacetyl)-, methyl ester is a chemical compound with the molecular formula C6H8F3NO4. It is a derivative of the naturally occurring amino acid L-serine, where the amino group is acylated with a trifluoroacetyl group and the carboxylic acid group is esterified with a methyl group. L-Serine, N-(trifluoroacetyl)-, methyl ester is often used in organic synthesis and as an intermediate in the preparation of various pharmaceuticals and agrochemicals. Its unique structure, featuring the trifluoroacetyl group, can enhance the reactivity and stability of the molecule, making it a valuable building block in the synthesis of complex organic compounds.

1604-45-1

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1604-45-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1604-45-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,6,0 and 4 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1604-45:
(6*1)+(5*6)+(4*0)+(3*4)+(2*4)+(1*5)=61
61 % 10 = 1
So 1604-45-1 is a valid CAS Registry Number.

1604-45-1SDS

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 methyl N-trifluoroacetylserinate

1.2 Other means of identification

Product number -
Other names (S)-3-Hydroxy-2-(2,2,2-trifluoro-acetylamino)-propionic acid methyl ester

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:1604-45-1 SDS

1604-45-1Upstream product

1604-45-1Relevant academic research and scientific papers

Convenient method for the kinetic resolution of β-aminoalcohols

Pelotier, Béatrice,Priem, Ghislaine,Macdonald, Simon J.F.,Anson, Mike S.,Upton, Richard J.,Campbell, Ian B.

, p. 9005 - 9007 (2007/10/03)

A variety of easily removable protecting groups were tested in the kinetic resolution of N-protected β-aminoalcohols using chiral catalysts derived from N-4′-pyridinyl-α-methyl proline. The trifluoroacetyl group was the most promising protecting group as it gave the highest selectivities with all alcohols tested and can easily be removed without loss of enantiomeric excess. This strategy constitutes a convenient method for the kinetic resolution of β-aminoalcohols.

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