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(1S,4R)-5-Oxo-bicyclo[2.2.1]hept-2-ene-7-carboxylic acid is a complex organic compound with the molecular formula C9H10O3. 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 4R configurations indicating the orientation of its substituents in three-dimensional space. This bicyclic compound features a seven-membered ring with a double bond and a carboxylic acid group, which gives it acidic properties. It is an important intermediate in the synthesis of various pharmaceuticals and natural products due to its unique structure and reactivity. The compound's oxo group (carbonyl) at the 5-position and the carboxylic acid at the 7-position contribute to its chemical reactivity and potential applications in organic synthesis.

64248-19-7

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64248-19-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 64248-19-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,4,2,4 and 8 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 64248-19:
(7*6)+(6*4)+(5*2)+(4*4)+(3*8)+(2*1)+(1*9)=127
127 % 10 = 7
So 64248-19-7 is a valid CAS Registry Number.

64248-19-7Downstream Products

64248-19-7Relevant academic research and scientific papers

ENANTIOSELECTIVE MICROBIAL HYDROXYLATION OF BICYCLOHEPTANE CARBON SKELETON

Yamazaki, Yoshimitsu,Maeda, Hidekatsu

, p. 4775 - 4776 (1985)

Bicycloheptane-7-carboxylic acid (1) and methyl bicyclohept-2-ene-7-syn-carboxylate (5) were microbiologically hydroxylated to give (1R)-2-hydroxy derivatives.

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