Cas 91465-20-2,(4E,8E)-(1S,2S,12R,13S,16R)-2,12-Dihydroxy-4,8,12-trimethyl-16-phenylsulfanylmethyl-14-oxa-bicyclo[11.3.1]heptadeca-4,8-dien-15-one

91465-20-2

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Basic information

Product Name: (4E,8E)-(1S,2S,12R,13S,16R)-2,12-Dihydroxy-4,8,12-trimethyl-16-phenylsulfanylmethyl-14-oxa-bicyclo[11.3.1]heptadeca-4,8-dien-15-one
Synonyms: (4E,8E)-(1S,2S,12R,13S,16R)-2,12-Dihydroxy-4,8,12-trimethyl-16-phenylsulfanylmethyl-14-oxa-bicyclo[11.3.1]heptadeca-4,8-dien-15-one
CAS NO:91465-20-2
Molecular Formula:
Molecular Weight: 444.635
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: (4E,8E)-(1S,2S,12R,13S,16R)-2,12-Dihydroxy-4,8,12-trimethyl-16-phenylsulfanylmethyl-14-oxa-bicyclo[11.3.1]heptadeca-4,8-dien-15-one(CAS DataBase Reference)
NIST Chemistry Reference: (4E,8E)-(1S,2S,12R,13S,16R)-2,12-Dihydroxy-4,8,12-trimethyl-16-phenylsulfanylmethyl-14-oxa-bicyclo[11.3.1]heptadeca-4,8-dien-15-one(91465-20-2)
EPA Substance Registry System: (4E,8E)-(1S,2S,12R,13S,16R)-2,12-Dihydroxy-4,8,12-trimethyl-16-phenylsulfanylmethyl-14-oxa-bicyclo[11.3.1]heptadeca-4,8-dien-15-one(91465-20-2)

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: 91465-20-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 91465-20-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,1,4,6 and 5 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 91465-20:
(7*9)+(6*1)+(5*4)+(4*6)+(3*5)+(2*2)+(1*0)=132
132 % 10 = 2
So 91465-20-2 is a valid CAS Registry Number.

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91465-20-2Relevant academic research and scientific papers

Interconversion of Cembranolide &δ- and &γ-Lactones: Synthesis of the C-1 Epimer of Isolobophytolide

Marshall, James A.,Karas, Lawrence J.,Coghlan, Michael J.

, p. 699 - 701 (2007/10/02)

The δ-lactone cembranolide diterpene crassin alcohol (2) has been converted to an isomeric γ-lactone isocrassin alcohol (6) by a sequence involving kinetically controlled addition of benzenethiol to the conjugated lactone double bond followed by base-prom

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