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(1S,4R,7S)-7-Benzyloxymethyl-bicyclo[2.2.1]hept-5-en-2-one is a complex organic compound with a molecular formula of C16H17O2. It features a bicyclic structure with a hept-5-en-2-one core, which consists of seven carbon atoms arranged in a bridged ring system. The compound has three chiral centers at positions 1, 4, and 7, with the specific configuration being S (for 1 and 7) and R (for 4). A benzyloxymethyl group is attached to the 7th carbon, which further contributes to the molecule's complexity. (1S,4R,7S)-7-Benzyloxymethyl-bicyclo[2.2.1]hept-5-en-2-one is of interest in organic chemistry and may have potential applications in the synthesis of pharmaceuticals or other specialty chemicals due to its unique structure and stereochemistry.

53176-69-5

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53176-69-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 53176-69-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,1,7 and 6 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 53176-69:
(7*5)+(6*3)+(5*1)+(4*7)+(3*6)+(2*6)+(1*9)=125
125 % 10 = 5
So 53176-69-5 is a valid CAS Registry Number.

53176-69-5Downstream Products

53176-69-5Relevant academic research and scientific papers

Asymmetric microbiological Baeyer-Villiger reaction of a bridged bicyclic ketone: Divergent behaviour of its enantiomers

Konigsberger,Alphand,Furstoss,Griengl

, p. 499 - 500 (2007/10/02)

The bioconversion of 7-anti-benzyloxymethylbicyclo[2.2.1]hept-5-en-2-one 1 with cells of Acinetobacter calcoaceticus NCIB 9871 has been studied. Its (1R,4S,7R) enantiomer underwent a Baeyer-Villiger oxidation yielding rearranged lactone 2 (ee 85%), whereas (1S,4R,7S)-1 was reduced to alcohols 3-endo (ee 95%) and 3-exo (o.p. 89%).

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