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(S)-2-(2,2,2-trifluoroacetamido)pentanoic acid is a chiral compound with the molecular formula C7H10F3NO4. It is a derivative of pentanoic acid, featuring a 2,2,2-trifluoroacetyl group attached to the amino group, and the (S)-configuration indicates that the hydroxyl group is positioned on the left side when looking at the molecule from the perspective of the carbon chain. (S)-2-(2,2,2-trifluoroacetamido)pentanoic acid is known for its potential applications in pharmaceuticals, particularly as a building block in the synthesis of various drugs. Its unique structure, with the trifluoroacetyl group, may confer specific properties that are beneficial for medicinal chemistry, such as enhanced metabolic stability or improved binding affinity to target proteins. The synthesis and use of (S)-2-(2,2,2-trifluoroacetamido)pentanoic acid in drug development highlight the importance of chiral chemistry in creating effective and selective therapeutic agents.

350-21-0

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350-21-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 350-21-0 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,5 and 0 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 350-21:
(5*3)+(4*5)+(3*0)+(2*2)+(1*1)=40
40 % 10 = 0
So 350-21-0 is a valid CAS Registry Number.

350-21-0Downstream Products

350-21-0Relevant academic research and scientific papers

Synthesis of chiral TFA-protected α-amino aryl-ketone derivatives with friedel-crafts acylation of α-amino acid n-hydroxysuccinimide ester

Tachrim, Zetryana Puteri,Oida, Kazuhiro,Ikemoto, Haruka,Ohashi, Fumina,Kurokawa, Natsumi,Hayashi, Kento,Shikanai, Mami,Sakihama, Yasuko,Hashidoko, Yasuyuki,Hashimoto, Makoto

, (2017)

Chiral N-protected α-amino aryl-ketones are one of the useful precursors used in the synthesis of various biologically active compounds and can be constructed via Friedel-Crafts acylation of N-protected α-amino acids. One of the drawbacks of this reaction

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