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N-TRIFLUOROACETYL-L-CYSTEINE METHYL ESTER is a chemical compound that is a methyl ester derivative of N-trifluoroacetyl-L-cysteine, an amino acid derivative. It is characterized by its ability to modify and bind to proteins, making it a valuable tool in the research and pharmaceutical industries for the synthesis of various pharmaceuticals and drug compounds. Its unique properties also allow it to be used as a building block in the synthesis of various organic compounds, with potential therapeutic applications.

1577-62-4

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1577-62-4 Usage

Uses

Used in Pharmaceutical Industry:
N-TRIFLUOROACETYL-L-CYSTEINE METHYL ESTER is used as a key intermediate in the synthesis of pharmaceuticals and drug compounds for its ability to modify and bind to proteins. This property aids in the development of new drugs with specific protein targets, potentially leading to more effective treatments for various diseases.
Used in Research Applications:
In the research field, N-TRIFLUOROACETYL-L-CYSTEINE METHYL ESTER is used as a reagent for studying protein structures, interactions, and functions. Its ability to bind to proteins allows researchers to gain insights into the mechanisms of protein folding, stability, and interactions with other biomolecules, contributing to a better understanding of biological processes and the development of novel therapeutic strategies.
Used in Organic Synthesis:
N-TRIFLUOROACETYL-L-CYSTEINE METHYL ESTER is used as a building block in the synthesis of various organic compounds. Its unique structure and reactivity make it a valuable component in the creation of complex organic molecules, which can be used in a wide range of applications, including the development of new materials, catalysts, and pharmaceuticals.
Used in Therapeutic Applications:
Although still under investigation, N-TRIFLUOROACETYL-L-CYSTEINE METHYL ESTER may have potential therapeutic applications due to its ability to modify and bind to proteins. Its potential use in the development of targeted therapies for various diseases is an area of ongoing research, with the aim of discovering new treatments that can specifically address the underlying molecular mechanisms of these conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 1577-62-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,5,7 and 7 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1577-62:
(6*1)+(5*5)+(4*7)+(3*7)+(2*6)+(1*2)=94
94 % 10 = 4
So 1577-62-4 is a valid CAS Registry Number.
InChI:InChI=1/C6H8F3NO3S/c1-13-4(11)3(2-14)10-5(12)6(7,8)9/h3,14H,2H2,1H3,(H,10,12)

1577-62-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name N-Trifluoroacetyl-L-cysteine methyl ester

1.2 Other means of identification

Product number -
Other names N-TFA-Cys-OCH3

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:1577-62-4 SDS

1577-62-4Relevant academic research and scientific papers

Cycloforskamide, a cytotoxic macrocyclic peptide from the sea slug Pleurobranchus forskalii

Tan, Karen Co,Wakimoto, Toshiyuki,Takada, Kentaro,Ohtsuki, Takashi,Uchiyama, Nahoko,Goda, Yukihiro,Abe, Ikuro

, p. 1388 - 1391 (2013/08/23)

A macrocylic dodecapeptide, cycloforskamide, was isolated from the sea slug Pleurobranchus forskalii, collected off Ishigaki Island, Japan. Its planar structure was deduced by extensive NMR analyses and was further confirmed by MS/MS fragmentation analyses. Finally, the absolute configuration was determined by total hydrolysis and chiral-phase gas chromatographic analysis. This novel dodecapeptide contains three d-amino acids and three thiazoline heterocycles and exhibits cytotoxicity against murine leukemia P388 cells, with an IC 50 of 5.8 μM.

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