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(1R,2S)-2-(1-Phenylsulfanyl-ethyl)-cyclopent-3-enecarboxylic acid is a complex organic compound with a molecular formula of C16H18O2S. It features a cyclopentane ring with a carboxylic acid group at the 3-position, an ethyl group at the 2-position, and a phenylsulfanyl group attached to the ethyl group. The compound has two chiral centers, with the R configuration at the 1-position and the S configuration at the 2-position. This chirality plays a crucial role in its biological activity and potential applications. The phenylsulfanyl group adds a sulfur-phenyl moiety to the molecule, which can influence its reactivity and interactions with other molecules. (1R,2S)-2-(1-Phenylsulfanyl-ethyl)-cyclopent-3-enecarboxylic acid may be of interest in the fields of pharmaceuticals, materials science, and organic chemistry due to its unique structure and potential for functionalization.

69765-63-5

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69765-63-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 69765-63-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,7,6 and 5 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 69765-63:
(7*6)+(6*9)+(5*7)+(4*6)+(3*5)+(2*6)+(1*3)=185
185 % 10 = 5
So 69765-63-5 is a valid CAS Registry Number.

69765-63-5Downstream Products

69765-63-5Relevant academic research and scientific papers

VICINAL ALKYLATION OF OLEFINS, REGIO- AND STEREOSELECTIVE ADDITION OF M + CN> UNITS TO CYCLOPENTADIENE.

Michel, P.,O'Donnell, M.,Biname, R.,Hesbain-Frisque, A.M.,Ghosez, L.,et al.

, p. 2577 - 2580 (2007/10/02)

Adducts of alkyl(phenylthio)ketenes to cyclopentadiene are cleaved with KOH-t-BuOK with retention of configuration at three centers.This observation broadens the synthetic potential of the method of vicinal alkylation of olefins.This method has been used for the vicinal addition of m + Cn> units to cyclopentadiene.

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