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(3S)-3-AMINO-3-(2,4,5-TRIFLUOROPHENYL)PROPANOIC ACID is a white crystalline powder with a molecular formula C9H9F3NO2. It is an amino acid derivative that contains a 2,4,5-trifluorophenyl group. (3S)-3-AMINO-3-(2,4,5-TRIFLUOROPHENYL)PROPANOIC ACID has potential applications in pharmaceutical and research settings, as it may have interactions with biological systems, particularly in the treatment of neurological disorders or as a potential building block for more complex molecules. Further studies are necessary to fully understand the properties and potential uses of (3S)-3-AMINO-3-(2,4,5-TRIFLUOROPHENYL)PROPANOIC ACID.

1269963-27-0

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1269963-27-0 Usage

Uses

Used in Pharmaceutical Industry:
(3S)-3-AMINO-3-(2,4,5-TRIFLUOROPHENYL)PROPANOIC ACID is used as a potential therapeutic agent for the treatment of neurological disorders. Its unique structure and interactions with biological systems may contribute to the development of new drugs or therapies for these conditions.
Used in Research Applications:
(3S)-3-AMINO-3-(2,4,5-TRIFLUOROPHENYL)PROPANOIC ACID is used as a research compound to study its interactions with biological systems and explore its potential applications in various fields. This may include the development of new drugs, the study of its effects on specific biological pathways, or as a building block for more complex molecules.

Check Digit Verification of cas no

The CAS Registry Mumber 1269963-27-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,6,9,9,6 and 3 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1269963-27:
(9*1)+(8*2)+(7*6)+(6*9)+(5*9)+(4*6)+(3*3)+(2*2)+(1*7)=210
210 % 10 = 0
So 1269963-27-0 is a valid CAS Registry Number.

1269963-27-0Downstream Products

1269963-27-0Relevant academic research and scientific papers

Asymmetric synthesis of β-fluoroaryl-β-amino acids

Davies, Stephen G.,Fletcher, Ai M.,Lv, Linlu,Roberts, Paul M.,Thomson, James E.

, p. 910 - 925 (2012/09/22)

The conjugate addition of lithium (R)-N-benzyl-N-(α-methylbenzyl) amide to a range of β-fluoroaryl-α,β-unsaturated esters gave the corresponding β-amino esters with high diastereoselectivity and in good isolated yields. Sequential treatment of the resulta

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