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(S)-4-Propyloxazolidine-2,5-dione, with the molecular formula C5H7NO3, is a cyclic urea derivative that serves as a key component in the synthesis of pharmaceuticals and agrochemicals. As a chiral molecule, it possesses a non-superimposable mirror image and can exist in two enantiomeric forms. The (S)-enantiomer has garnered attention for its potential biological activities, particularly in the synthesis of alpha-amino acids and peptides, as well as its possible anticonvulsant and anxiolytic effects, making it a compound of interest in medicinal chemistry.

1676-87-5

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1676-87-5 Usage

Uses

Used in Pharmaceutical Synthesis:
(S)-4-Propyloxazolidine-2,5-dione is used as a key intermediate in the synthesis of various pharmaceuticals, contributing to the development of new drugs and therapies.
Used in Agrochemical Synthesis:
(S)-4-Propyloxazolidine-2,5-dione is also utilized as a building block in the creation of agrochemicals, playing a role in the development of products for agricultural applications.
Used in Medicinal Chemistry:
(S)-4-Propyloxazolidine-2,5-dione is used as a chiral molecule for the synthesis of alpha-amino acids and peptides, which are essential components in the development of new medications.
Used in the Study of Biological Activities:
(S)-4-Propyloxazolidine-2,5-dione is employed in research as a potential anticonvulsant and anxiolytic agent, aiming to develop treatments for seizure disorders and anxiety-related conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 1676-87-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,6,7 and 6 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1676-87:
(6*1)+(5*6)+(4*7)+(3*6)+(2*8)+(1*7)=105
105 % 10 = 5
So 1676-87-5 is a valid CAS Registry Number.

1676-87-5Relevant academic research and scientific papers

The biosynthetic origin of diketopiperazines derived from D-proline

Bull, Steven D.,Davies, Stephen G.,Parkin, Richard M.,Sanchez-Sancho, Francisco

, p. 2313 - 2320 (2007/10/03)

Investigations reveal that the structures assigned to D-α-amino acid containing diketopiperazines (DKPs) 21-25 isolated from the sponge Calyx CF. podatypa have been reported incorrectly. Synthetic studies and comparison with literature data have enabled the structures of these DKPs to be correctly reassigned. Evidence is presented to suggest that naturally occurring D-Pro-L-Xxx-DKPs are artifacts resulting from non-enzymatic epimerisation of the corresponding L-Pro-L-Xxx-DKP natural products.

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