Cas 65516-41-8,(2R,3S)-3-Benzenesulfonyl-2-((3aR,5aS,6S,10R,10aR)-10-methoxy-3a,5a-dimethyl-hexadecahydro-cyclopenta[a]cyclopropa[2,3]cyclopenta[1,2-f]naphthalen-6-yl)-2-methyl-oxirane

65516-41-8

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Basic information

Product Name: (2R,3S)-3-Benzenesulfonyl-2-((3aR,5aS,6S,10R,10aR)-10-methoxy-3a,5a-dimethyl-hexadecahydro-cyclopenta[a]cyclopropa[2,3]cyclopenta[1,2-f]naphthalen-6-yl)-2-methyl-oxirane
Synonyms:
CAS NO:65516-41-8
Molecular Formula:
Molecular Weight: 484.7
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: (2R,3S)-3-Benzenesulfonyl-2-((3aR,5aS,6S,10R,10aR)-10-methoxy-3a,5a-dimethyl-hexadecahydro-cyclopenta[a]cyclopropa[2,3]cyclopenta[1,2-f]naphthalen-6-yl)-2-methyl-oxirane(CAS DataBase Reference)
NIST Chemistry Reference: (2R,3S)-3-Benzenesulfonyl-2-((3aR,5aS,6S,10R,10aR)-10-methoxy-3a,5a-dimethyl-hexadecahydro-cyclopenta[a]cyclopropa[2,3]cyclopenta[1,2-f]naphthalen-6-yl)-2-methyl-oxirane(65516-41-8)
EPA Substance Registry System: (2R,3S)-3-Benzenesulfonyl-2-((3aR,5aS,6S,10R,10aR)-10-methoxy-3a,5a-dimethyl-hexadecahydro-cyclopenta[a]cyclopropa[2,3]cyclopenta[1,2-f]naphthalen-6-yl)-2-methyl-oxirane(65516-41-8)

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: 65516-41-8(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 65516-41-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,5,1 and 6 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 65516-41:
(7*6)+(6*5)+(5*5)+(4*1)+(3*6)+(2*4)+(1*1)=128
128 % 10 = 8
So 65516-41-8 is a valid CAS Registry Number.

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65516-41-8Relevant academic research and scientific papers

A New Procedure for the One-Carbon Homologation of Ketones to α-Hydroxy Aldehydes

Adamczyk, Maciej,Dolence, E. Kurt,Watt, David S.,Christy, M. Robert,Reibenspies, Joseph H.,Anderson, Oren P.

, p. 1378 - 1382 (1984)

A new, one-carbon homologation procedure for the conversion of ketones to α-hydroxy aldehydes involves two steps: (1) Darzens condensation of ketones with chloromethyl phenyl sulfone; (2) ring opening of the intermediate α,β-epoxy sulfones with hydroxide

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