Cas 64798-81-8,(6α,6aβ,9α,9bβ)-5,6,6a,7,8,9a,9b-octahydro-6,9a-dimethyl-9-(phenylmethoxy)azuleno<4,5-b>furan-2(4H)-one

64798-81-8

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Basic information

Product Name: (6α,6aβ,9α,9bβ)-5,6,6a,7,8,9a,9b-octahydro-6,9a-dimethyl-9-(phenylmethoxy)azuleno<4,5-b>furan-2(4H)-one
Synonyms: (6α,6aβ,9α,9bβ)-5,6,6a,7,8,9a,9b-octahydro-6,9a-dimethyl-9-(phenylmethoxy)azuleno<4,5-b>furan-2(4H)-one
CAS NO:64798-81-8
Molecular Formula:
Molecular Weight: 326.436
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: (6α,6aβ,9α,9bβ)-5,6,6a,7,8,9a,9b-octahydro-6,9a-dimethyl-9-(phenylmethoxy)azuleno<4,5-b>furan-2(4H)-one(CAS DataBase Reference)
NIST Chemistry Reference: (6α,6aβ,9α,9bβ)-5,6,6a,7,8,9a,9b-octahydro-6,9a-dimethyl-9-(phenylmethoxy)azuleno<4,5-b>furan-2(4H)-one(64798-81-8)
EPA Substance Registry System: (6α,6aβ,9α,9bβ)-5,6,6a,7,8,9a,9b-octahydro-6,9a-dimethyl-9-(phenylmethoxy)azuleno<4,5-b>furan-2(4H)-one(64798-81-8)

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: 64798-81-8(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 64798-81-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,4,7,9 and 8 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 64798-81:
(7*6)+(6*4)+(5*7)+(4*9)+(3*8)+(2*8)+(1*1)=178
178 % 10 = 8
So 64798-81-8 is a valid CAS Registry Number.

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64798-81-8Relevant academic research and scientific papers

Pseudoguaianolides. 1. Stereospecific Total Synthesis of the Ambrosanolides dl-Ambrosin and dl-Damsin

Grieco, Paul A.,Majetich, George F.,Ohfune, Yasufumi

, p. 4226 - 4233 (2007/10/02)

Regio- and stereospecific total syntheses of the sesquiterpene lactones dl-ambrosin (1) and dl-damsin (2) are described.Both syntheses start with bromo ketal ester 8 and proceed via the intermediacy of cyclopentenol 4, the precursor to perhydroazulenone 2

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