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Methyl 3,3,3-trifluoroalaninate is a chemical compound with the molecular formula C4H6F3NO2. It is a derivative of alanine, an amino acid commonly found in proteins. Characterized by the presence of three fluorine atoms attached to the carbon atom in the alanine molecule, Methyl 3,3,3-trifluoroalaninate imparts unique chemical and physical properties. Methyl 3,3,3-trifluoroalaninate is often utilized in organic synthesis as a building block for the production of various pharmaceuticals, agrochemicals, and materials. Additionally, it serves as a precursor for the synthesis of fluorinated amino acids, which are significant in medicinal chemistry and drug development. The fluorinated nature of Methyl 3,3,3-trifluoroalaninate may confer different reactivity and biological activity compared to its non-fluorinated counterparts, rendering it a valuable asset in chemical research and development.

27240-44-4

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27240-44-4 Usage

Uses

Used in Pharmaceutical Industry:
Methyl 3,3,3-trifluoroalaninate is used as a building block for the synthesis of various pharmaceuticals due to its unique chemical and physical properties. The presence of fluorine atoms can enhance the reactivity and biological activity of the resulting compounds, making them more effective in treating various medical conditions.
Used in Agrochemical Industry:
In the agrochemical industry, Methyl 3,3,3-trifluoroalaninate is used as a precursor for the development of new agrochemicals. The incorporation of fluorine atoms can improve the stability, efficacy, and selectivity of these compounds, leading to more effective pest control and crop protection.
Used in Materials Science:
Methyl 3,3,3-trifluoroalaninate is utilized in materials science for the synthesis of novel materials with unique properties. The fluorinated nature of Methyl 3,3,3-trifluoroalaninate can contribute to the development of materials with enhanced thermal stability, chemical resistance, and other desirable characteristics.
Used in Medicinal Chemistry:
Methyl 3,3,3-trifluoroalaninate is used as a precursor for the synthesis of fluorinated amino acids in medicinal chemistry. These fluorinated amino acids can be incorporated into peptide and protein structures, potentially leading to the development of new drugs with improved pharmacokinetic and pharmacodynamic properties.
Used in Drug Development:
In drug development, Methyl 3,3,3-trifluoroalaninate serves as a valuable tool for the synthesis of new drug candidates. The unique properties of Methyl 3,3,3-trifluoroalaninate, such as its reactivity and biological activity, can be harnessed to design and develop innovative therapeutic agents with improved efficacy and safety profiles.

Check Digit Verification of cas no

The CAS Registry Mumber 27240-44-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,7,2,4 and 0 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 27240-44:
(7*2)+(6*7)+(5*2)+(4*4)+(3*0)+(2*4)+(1*4)=94
94 % 10 = 4
So 27240-44-4 is a valid CAS Registry Number.
InChI:InChI=1/C4H6F3NO2.ClH/c1-10-3(9)2(8)4(5,6)7;/h2H,8H2,1H3;1H

27240-44-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 2-amino-3,3,3-trifluoropropanoate

1.2 Other means of identification

Product number -
Other names 3,3,3-Trifluor-alanin-methylester

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:27240-44-4 SDS

27240-44-4Downstream Products

27240-44-4Relevant academic research and scientific papers

New Synthetic Pathways to 3,3,3-Trifluoroalanine, 2-Deutero-3,3,3-trifluoroalanine and their Derivatives

Burger, Klaus,Hoess, Eva,Gaa, Karl,Sewald, Norbert,Schierlinger, Christian

, p. 361 - 384 (2007/10/02)

New synthetic pathways to 3,3,3-trifluoroalanine, 2-deutero-3,3,3-trifluoroalanine, their esters, amides, and thioamides are described, starting from hexafluoroacetone, and trifluoropyruvates, respectively.

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