Cas 1208239-73-9,(1R,6S,8S)-5-allyl-8-benzyloxy-4,6,9,9-tetramethylbicyclo[4.3.0]non-4-en-3-one

1208239-73-9

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Basic information

Product Name: (1R,6S,8S)-5-allyl-8-benzyloxy-4,6,9,9-tetramethylbicyclo[4.3.0]non-4-en-3-one
Synonyms: (1R,6S,8S)-5-allyl-8-benzyloxy-4,6,9,9-tetramethylbicyclo[4.3.0]non-4-en-3-one
CAS NO:1208239-73-9
Molecular Formula:
Molecular Weight: 338.49
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: (1R,6S,8S)-5-allyl-8-benzyloxy-4,6,9,9-tetramethylbicyclo[4.3.0]non-4-en-3-one(CAS DataBase Reference)
NIST Chemistry Reference: (1R,6S,8S)-5-allyl-8-benzyloxy-4,6,9,9-tetramethylbicyclo[4.3.0]non-4-en-3-one(1208239-73-9)
EPA Substance Registry System: (1R,6S,8S)-5-allyl-8-benzyloxy-4,6,9,9-tetramethylbicyclo[4.3.0]non-4-en-3-one(1208239-73-9)

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: 1208239-73-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1208239-73-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,0,8,2,3 and 9 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1208239-73:
(9*1)+(8*2)+(7*0)+(6*8)+(5*2)+(4*3)+(3*9)+(2*7)+(1*3)=139
139 % 10 = 9
So 1208239-73-9 is a valid CAS Registry Number.

1208239-73-9Upstream product

1208239-72-8 (1S,2S,6S,8S)-2-allyl-8-benzyloxy-1,3,7,7-tetramethylbicyclo[4.3.0]non-3-en-2-ol

1208239-73-9Downstream Products

1208239-73-9Relevant academic research and scientific papers

Enantiospecific synthesis of ABC-ring system of A-nor and abeo 4(3→2) tetra and pentacyclic triterpenes

Srikrishna,Babu, R. Ramesh,Beeraiah

experimental part, p. 852 - 861 (2010/03/24)

Enantiospecific synthesis of ABC-ring systems of A-nor and abeo 4(3→2) tetra and pentacyclic triterpenes has been accomplished starting from the readily available monoterpene (R)-carvone. (R)-Carvone was used as the B-ring of the target molecules. A lithi

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