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5317-15-7

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5317-15-7 Usage

Description

(4R)-3-(tert-butoxycarbonyl)-2,2-dimethylthiazolidine-4-carboxylic acid is a chiral chemical compound that belongs to the thiazolidine-4-carboxylic acid family. It features a four-membered thiazolidine ring and a carboxylic acid group, with a tert-butoxycarbonyl (Boc) protecting group attached to the nitrogen atom. This structure makes it a versatile compound for various applications in organic synthesis, medicinal chemistry, and pharmaceutical research.

Uses

Used in Organic Synthesis:
(4R)-3-(tert-butoxycarbonyl)-2,2-dimethylthiazolidine-4-carboxylic acid is used as a building block for the synthesis of complex organic molecules, taking advantage of its reactive functional groups and chiral center.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, (4R)-3-(tert-butoxycarbonyl)-2,2-dimethylthiazolidine-4-carboxylic acid is used as a key intermediate in the development of novel pharmaceuticals, potentially leading to new drugs with improved efficacy and selectivity.
Used in Pharmaceutical Research:
(4R)-3-(tert-butoxycarbonyl)-2,2-dimethylthiazolidine-4-carboxylic acid is used as a research compound for studying its biological effects and properties, which may contribute to the discovery of new therapeutic targets and treatments.
Used in Peptide Synthesis:
Due to the presence of the Boc protecting group, (4R)-3-(tert-butoxycarbonyl)-2,2-dimethylthiazolidine-4-carboxylic acid is used as a protected amino acid in peptide synthesis, facilitating the formation of peptide bonds and protecting the carboxylic acid group from unwanted reactions during the synthesis process.
Used in the Development of Drug Delivery Systems:
(4R)-3-(tert-butoxycarbonyl)-2,2-dimethylthiazolidine-4-carboxylic acid may also be used in the design and development of drug delivery systems, leveraging its chemical structure to improve the solubility, stability, and targeted delivery of therapeutic agents.
Used in Chemical Reactivity Studies:
(4R)-3-(tert-butoxycarbonyl)-2,2-dimethylthiazolidine-4-carboxylic acid can be employed in studies aimed at understanding its reactivity with various reagents, which could provide insights into new reaction mechanisms and synthetic strategies.

Check Digit Verification of cas no

The CAS Registry Mumber 5317-15-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,3,1 and 7 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 5317-15:
(6*5)+(5*3)+(4*1)+(3*7)+(2*1)+(1*5)=77
77 % 10 = 7
So 5317-15-7 is a valid CAS Registry Number.

5317-15-7Upstream product

5317-15-7Downstream Products

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