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(R)-2-Benzyloxycarbonylamino-3-thiazol-4-yl-propionic acid is a compound with a molecular formula of C16H16N2O4S and a molecular weight of 332.37 g/mol. It is a derivative of thiazole and propionic acid, containing a thiazole ring and a propionic acid side chain. This chemical is characterized by its potential biological activity, which includes antibacterial and antifungal properties, and its utility as a chiral auxiliary in asymmetric synthesis, where its stereochemistry can significantly influence the outcomes of chemical reactions.

119817-29-7

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119817-29-7 Usage

Uses

Used in Pharmaceutical Research:
(R)-2-Benzyloxycarbonylamino-3-thiazol-4-yl-propionic acid is used as a building block in pharmaceutical research for the development of new drugs. Its unique structure and biological activity make it a valuable component in the creation of novel therapeutic agents.
Used in Organic Synthesis:
In the field of organic synthesis, (R)-2-Benzyloxycarbonylamino-3-thiazol-4-yl-propionic acid is used as a key component in the synthesis of various complex organic molecules. Its versatility and reactivity contribute to the advancement of chemical research and the development of new compounds with potential applications.
Used as a Chiral Auxiliary:
(R)-2-Benzyloxycarbonylamino-3-thiazol-4-yl-propionic acid is used as a chiral auxiliary in asymmetric synthesis. Its stereochemistry plays a crucial role in determining the selectivity and outcome of chemical reactions, which is essential for the production of enantiomerically pure compounds with specific biological activities.
Used in Antimicrobial Applications:
Due to its demonstrated antibacterial and antifungal properties, (R)-2-Benzyloxycarbonylamino-3-thiazol-4-yl-propionic acid is used in the development of antimicrobial agents. These agents can be employed in various industries, such as healthcare and agriculture, to combat microbial infections and protect crops from diseases.

Check Digit Verification of cas no

The CAS Registry Mumber 119817-29-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,9,8,1 and 7 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 119817-29:
(8*1)+(7*1)+(6*9)+(5*8)+(4*1)+(3*7)+(2*2)+(1*9)=147
147 % 10 = 7
So 119817-29-7 is a valid CAS Registry Number.

119817-29-7Relevant academic research and scientific papers

Porcine Pancreatic Lipase Catalyzed Enantioselective Hydrolysis of Esters of N-Protected Unusual Amino Acids

Miyazawa, Toshifumi,Iwanaga, Hitoshi,Ueji, Shinichi,Yamada,Takashi,Kuwata, Shigeru

, p. 2219 - 2222 (2007/10/02)

Porcine pancreatic lipase catalyzed the highly enantioselective hydrolysis of a kind of α-substituted carboxylic esters, i.e., the 2,2,2-trifluoroethyl esters of the N-benzyloxycarbonyl derivatives of unusual amino acids.

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