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(3R)-3-[(1R)-1-phenylethylamino]-4-(2,4,5-trifluorophenyl)butanoic acid is a complex organic compound with a butanoic acid backbone, featuring a substituted phenyl group and an amino group. Its stereochemistry, denoted by the (3R) and (1R) configurations, indicates a specific orientation of its functional groups. The presence of a trifluorophenyl group and a phenylethylamino group suggests potential pharmaceutical applications and interactions with biological systems or targets within the body, making it a compound of interest for further study in medicinal chemistry or pharmacology.

1345822-99-2

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1345822-99-2 Usage

Uses

Used in Pharmaceutical Industry:
(3R)-3-[(1R)-1-phenylethylamino]-4-(2,4,5-trifluorophenyl)butanoic acid is used as a potential pharmaceutical agent for [specific therapeutic area] due to its unique structural features and the presence of fluoro-substituted and phenylethylamino groups, which may contribute to its interaction with biological targets and its potential efficacy in treating [specific condition or disease].

Check Digit Verification of cas no

The CAS Registry Mumber 1345822-99-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,4,5,8,2 and 2 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1345822-99:
(9*1)+(8*3)+(7*4)+(6*5)+(5*8)+(4*2)+(3*2)+(2*9)+(1*9)=172
172 % 10 = 2
So 1345822-99-2 is a valid CAS Registry Number.

1345822-99-2Downstream Products

1345822-99-2Relevant academic research and scientific papers

Preparation method and intermediate of beta-substituted amino-gamma-substituted aryl butyric acid

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, (2018/02/04)

The invention discloses a preparation method and an intermediate of beta-substituted amino-gamma-substituted aryl butyric acid. Specifically, the preparation method comprises the steps that firstly, 2,4,5- trifluorophenylacetic acid is taken as a raw mate

PROCESS FOR THE PREPARATION OF CHIRAL BETA AMINO CARBOXAMIDE DERIVATIVES

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, (2011/11/13)

The present invention provides a process for preparing a compound of formula (I), or a pharmaceutically acceptable salt thereof, having the R-configuration, of formula (IA), or S-configuration of formula (IB), selectively over the other enantiomer.

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