Cas 117152-30-4,(3S,3aS,5aR,6S,8S,9bS)-6,8-Dihydroxy-3,5a,9-trimethyl-3a,4,5,5a,6,7,8,9b-octahydro-3H-naphtho[1,2-b]furan-2-one

117152-30-4

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Basic information

Product Name: (3S,3aS,5aR,6S,8S,9bS)-6,8-Dihydroxy-3,5a,9-trimethyl-3a,4,5,5a,6,7,8,9b-octahydro-3H-naphtho[1,2-b]furan-2-one
Synonyms:
CAS NO:117152-30-4
Molecular Formula:
Molecular Weight: 266.337
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: (3S,3aS,5aR,6S,8S,9bS)-6,8-Dihydroxy-3,5a,9-trimethyl-3a,4,5,5a,6,7,8,9b-octahydro-3H-naphtho[1,2-b]furan-2-one(CAS DataBase Reference)
NIST Chemistry Reference: (3S,3aS,5aR,6S,8S,9bS)-6,8-Dihydroxy-3,5a,9-trimethyl-3a,4,5,5a,6,7,8,9b-octahydro-3H-naphtho[1,2-b]furan-2-one(117152-30-4)
EPA Substance Registry System: (3S,3aS,5aR,6S,8S,9bS)-6,8-Dihydroxy-3,5a,9-trimethyl-3a,4,5,5a,6,7,8,9b-octahydro-3H-naphtho[1,2-b]furan-2-one(117152-30-4)

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: 117152-30-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 117152-30-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,7,1,5 and 2 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 117152-30:
(8*1)+(7*1)+(6*7)+(5*1)+(4*5)+(3*2)+(2*3)+(1*0)=94
94 % 10 = 4
So 117152-30-4 is a valid CAS Registry Number.

117152-30-4Upstream product

71327-31-6 dehydroisoerivanin

117152-30-4Downstream Products

117152-30-4Relevant academic research and scientific papers

Synthesis of Dehydroisoerivanin, Isoerivanin, Ludovicin C, and 1α,3α-Dihydroxyarbusculin B Utilizing the Organoselenium-mediated Reduction of Epoxy Ketone

Miyashita, Masaaki,Suzuki, Toshio,Yoshikoshi, Akira

, p. 2387 - 2390 (1987)

Short step synthesis of dehydroisoerivanin, isoerivanin, ludovicin C, and 1α,3α-dihydroxyarbusculin B have been achieved by employing the organoselenium-mediated reduction of α,β-epoxy ketone as the key step.

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