Cas 93943-52-3,4,8-epoxy-1,3,4,4a,5,6,7,7a,8,9-decahydro-1-hydroxy-6,6,8-trimethylazuleno<5,6-c>furan

93943-52-3

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Basic information

Product Name: 4,8-epoxy-1,3,4,4a,5,6,7,7a,8,9-decahydro-1-hydroxy-6,6,8-trimethylazuleno<5,6-c>furan
Synonyms:
CAS NO:93943-52-3
Molecular Formula:
Molecular Weight: 250.338
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: 4,8-epoxy-1,3,4,4a,5,6,7,7a,8,9-decahydro-1-hydroxy-6,6,8-trimethylazuleno<5,6-c>furan(CAS DataBase Reference)
NIST Chemistry Reference: 4,8-epoxy-1,3,4,4a,5,6,7,7a,8,9-decahydro-1-hydroxy-6,6,8-trimethylazuleno<5,6-c>furan(93943-52-3)
EPA Substance Registry System: 4,8-epoxy-1,3,4,4a,5,6,7,7a,8,9-decahydro-1-hydroxy-6,6,8-trimethylazuleno<5,6-c>furan(93943-52-3)

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: 93943-52-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 93943-52-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,3,9,4 and 3 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 93943-52:
(7*9)+(6*3)+(5*9)+(4*4)+(3*3)+(2*5)+(1*2)=163
163 % 10 = 3
So 93943-52-3 is a valid CAS Registry Number.

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93943-52-3Relevant academic research and scientific papers

Basidiomycete Sesquiterpenes: The Silica Gel Induced Degradation of Velutinal Derivatives

Sterner, Olov,Bergman, Rolf,Kihlberg, Jan,Oluwadiya, James,Wickberg, Boerje,et al.

, p. 950 - 953 (2007/10/02)

Derivatives of the pentacyclic sesquiterpene velutinal, occurring as fatty acid esters in Lactarius species and in other Basidiomycetes, from a number of previously isolated furanoid sesquiterpenes when degraded by silica gel.On the basis of the structure of isolated intermediates and products, a mechanism for the degradation is proposed.

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