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(3R)-5-oxo-1-[(1R)-1-phenylethyl]pyrrolidine-3-carbonitrile is a chiral pyrrolidine derivative with a molecular formula of C15H16N2O. It features a pyrrolidine ring with a phenylethyl group attached and a carbonitrile group, indicating potential applications in organic synthesis and medicinal chemistry.

1292289-47-4

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1292289-47-4 Usage

Uses

Used in Organic Synthesis:
(3R)-5-oxo-1-[(1R)-1-phenylethyl]pyrrolidine-3-carbonitrile is used as a synthetic intermediate for the development of various organic compounds. Its unique structure and functional groups make it a valuable building block in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Medicinal Chemistry:
(3R)-5-oxo-1-[(1R)-1-phenylethyl]pyrrolidine-3-carbonitrile is used as a lead compound in drug discovery for potential therapeutic applications. Its chiral nature and specific stereochemistry may contribute to its biological activity, making it a promising candidate for further research and development in the pharmaceutical industry.
Further research is needed to explore the potential biological and chemical properties of (3R)-5-oxo-1-[(1R)-1-phenylethyl]pyrrolidine-3-carbonitrile, as well as its applications in different industries.

Check Digit Verification of cas no

The CAS Registry Mumber 1292289-47-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,9,2,2,8 and 9 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1292289-47:
(9*1)+(8*2)+(7*9)+(6*2)+(5*2)+(4*8)+(3*9)+(2*4)+(1*7)=184
184 % 10 = 4
So 1292289-47-4 is a valid CAS Registry Number.

1292289-47-4Relevant academic research and scientific papers

Adamantyl Iminocarbonyl-Substituted Pyrimidines As Inhibitors Of 11-Beta-HSD1 826

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, (2011/05/03)

A compound of formula (I): and pharmaceutically-acceptable salts thereof, wherein the variable groups are defined within; their use in the inhibition of 11βHSD1, processes for making them and pharmaceutical compositions comprising them are also described

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