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1246960-25-7

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  • (R)-3-(((benzyloxy)carbonyl)amino)-4-(2,4,5-trifluorophenyl)butanoic acid

    Cas No: 1246960-25-7

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1246960-25-7 Usage

Description

(R)-3-(((Benzyloxy)carbonyl)amino)-4-(2,4,5-trifluorophenyl)butanoic acid is a complex organic molecule belonging to the amino acid family. It features a 4-carbon chain with a carboxylic acid group and a benzyl ester group attached to the third carbon. The terminal end of the chain is connected to an amino group, which is linked to a 2,4,5-trifluorophenyl group. (R)-3-(((benzyloxy)carbonyl)amino)-4-(2,4,5-trifluorophenyl)butanoic acid's unique structure, including the benzyl ester and trifluorophenyl groups, may provide it with specific chemical and biological properties, making it a valuable candidate for pharmaceutical or chemical research applications.

Uses

Used in Pharmaceutical Research:
(R)-3-(((Benzyloxy)carbonyl)amino)-4-(2,4,5-trifluorophenyl)butanoic acid is used as a key intermediate in the synthesis of various pharmaceutical compounds. Its unique structure allows for the development of new drugs targeting specific biological processes, potentially leading to novel treatments for various diseases.
Used in Chemical Research:
In the field of chemical research, (R)-3-(((benzyloxy)carbonyl)amino)-4-(2,4,5-trifluorophenyl)butanoic acid serves as a valuable compound for studying the effects of structural modifications on chemical and biological properties. This can lead to a better understanding of molecular interactions and the development of new chemical entities with improved characteristics.
Used in Drug Delivery Systems:
(R)-3-(((Benzyloxy)carbonyl)amino)-4-(2,4,5-trifluorophenyl)butanoic acid can be utilized in the development of drug delivery systems, where its unique structure may enhance the solubility, stability, or targeted delivery of therapeutic agents. This application can improve the bioavailability and efficacy of drugs, leading to more effective treatments for patients.
Used in Biochemical Studies:
As a member of the amino acid family, (R)-3-(((benzyloxy)carbonyl)amino)-4-(2,4,5-trifluorophenyl)butanoic acid can be employed in biochemical studies to investigate its interactions with proteins and other biomolecules. This research can provide insights into the role of amino acids in biological processes and contribute to the development of new therapeutic strategies.

Check Digit Verification of cas no

The CAS Registry Mumber 1246960-25-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,4,6,9,6 and 0 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1246960-25:
(9*1)+(8*2)+(7*4)+(6*6)+(5*9)+(4*6)+(3*0)+(2*2)+(1*5)=167
167 % 10 = 7
So 1246960-25-7 is a valid CAS Registry Number.

1246960-25-7Relevant articles and documents

Glucovance west Geleg sandbank intermediate process for the preparation of amino acid derivatives

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, (2019/02/02)

The invention discloses a preparation method of a new diabetes drug sitagliptin intermediate aminobenzene butyric acid derivative. The preparation method comprises the following steps of: (1) mixing a compound shown in a formula I with R(+)-alpha-phenethyl and acetic acid to obtain a compound shown in a formula II; (2) mixing the compound shown in the formula II with sodium borohydride and protonic acid or lewis acid to obtain a compound shown in a formula III; (3) mixing the compound shown in the formula III with X to obtain a compound shown in a formula IV; (4) mixing the compound as shown in the formula IV with an inorganic base 1 to obtain a compound shown in a formula V; (5) obtaining a compound shown in a formula VI by the compound shown in the formula V; and (6) mixing the compound shown in the formula VI with an inorganic base 2 to obtain a compound shown in a formula VII.

METHOD FOR PREPARING DIPEPTIDYL PEPTIDASE-IV INHIBITOR AND INTERMEDIATE

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, (2012/02/01)

The present invention relates to an improved method for preparing dipeptidyl peptidase-IV inhibitor and intermediate. The present invention is able to reduce preparation costs by using low cost reagents on reaction and is able to be used in mass production by improving yield.

Process for the production of sitagliptin

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Page/Page column 11-12, (2012/03/26)

The present invention is directed to a process for the preparation of Sitagliptin, having formula (I)

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