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(1S,5R)-2-Oxo-5-phenylselanylmethyl-cyclopentanecarboxylic acid methyl ester is a complex organic compound with the molecular formula C14H16O3Se. It is a chiral molecule, meaning it has a non-superimposable mirror image, and it is characterized by its specific stereochemistry, with the 1S and 5R configurations indicating the orientation of the phenylselanylmethyl group and the carbonyl group, respectively. (1S,5R)-2-Oxo-5-phenylselanylmethyl-cyclopentanecarboxylic acid methyl ester features a cyclopentane ring, a five-membered carbon ring, with a carbonyl group at position 2, a phenylselanylmethyl group at position 5, and a methyl ester group. The phenylselanylmethyl group introduces a selenium atom into the molecule, which can have unique chemical and biological properties compared to its sulfur-containing analogs. (1S,5R)-2-Oxo-5-phenylselanylmethyl-cyclopentanecarboxylic acid methyl ester may be of interest in the fields of organic synthesis, medicinal chemistry, and materials science due to its potential applications in the development of new drugs, agrochemicals, or other specialty chemicals.

76877-73-1

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76877-73-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 76877-73-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,8,7 and 7 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 76877-73:
(7*7)+(6*6)+(5*8)+(4*7)+(3*7)+(2*7)+(1*3)=191
191 % 10 = 1
So 76877-73-1 is a valid CAS Registry Number.

76877-73-1Downstream Products

76877-73-1Relevant academic research and scientific papers

Hexenyl Radical Cyclization via Phenyl Selenide Transfer

Byers, Jeffrey H.,Gleason, Thomas G.,Knight, Kyle S.

, p. 354 - 356 (2007/10/02)

Several 2-phenylseleno-1,3-dicarbonyl compounds have been shown to undergo radical cyclization accompanied by phenyl selenide transfer upon photolysis.

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