Cas 51262-71-6,(3aS,4R,6aR)-4-Benzyloxymethyl-3,3a,4,6a-tetrahydro-cyclopenta[b]furan-2-one

51262-71-6

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Basic information

Product Name: (3aS,4R,6aR)-4-Benzyloxymethyl-3,3a,4,6a-tetrahydro-cyclopenta[b]furan-2-one
Synonyms:
CAS NO:51262-71-6
Molecular Formula:
Molecular Weight: 244.29
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: (3aS,4R,6aR)-4-Benzyloxymethyl-3,3a,4,6a-tetrahydro-cyclopenta[b]furan-2-one(CAS DataBase Reference)
NIST Chemistry Reference: (3aS,4R,6aR)-4-Benzyloxymethyl-3,3a,4,6a-tetrahydro-cyclopenta[b]furan-2-one(51262-71-6)
EPA Substance Registry System: (3aS,4R,6aR)-4-Benzyloxymethyl-3,3a,4,6a-tetrahydro-cyclopenta[b]furan-2-one(51262-71-6)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 51262-71-6(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 51262-71-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,2,6 and 2 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 51262-71:
(7*5)+(6*1)+(5*2)+(4*6)+(3*2)+(2*7)+(1*1)=96
96 % 10 = 6
So 51262-71-6 is a valid CAS Registry Number.

51262-71-6Upstream product

51262-71-6Downstream Products

51262-71-6Relevant 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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