Cas 850161-08-9,(4RS)-3-(tert-butoxy)-4-hydroxy-2-methyl-4-{(3R,6S)-6-methyl-3-[(2S,4E)-2-methyl-4,6-heptadien-2-yl]-1-cyclohexenyl}-2-cyclobuten-1-one

850161-08-9

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Product Name: (4RS)-3-(tert-butoxy)-4-hydroxy-2-methyl-4-{(3R,6S)-6-methyl-3-[(2S,4E)-2-methyl-4,6-heptadien-2-yl]-1-cyclohexenyl}-2-cyclobuten-1-one
Synonyms: (4RS)-3-(tert-butoxy)-4-hydroxy-2-methyl-4-{(3R,6S)-6-methyl-3-[(2S,4E)-2-methyl-4,6-heptadien-2-yl]-1-cyclohexenyl}-2-cyclobuten-1-one
CAS NO:850161-08-9
Molecular Formula:
Molecular Weight: 372.548
EINECS: N/A
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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: (4RS)-3-(tert-butoxy)-4-hydroxy-2-methyl-4-{(3R,6S)-6-methyl-3-[(2S,4E)-2-methyl-4,6-heptadien-2-yl]-1-cyclohexenyl}-2-cyclobuten-1-one(CAS DataBase Reference)
NIST Chemistry Reference: (4RS)-3-(tert-butoxy)-4-hydroxy-2-methyl-4-{(3R,6S)-6-methyl-3-[(2S,4E)-2-methyl-4,6-heptadien-2-yl]-1-cyclohexenyl}-2-cyclobuten-1-one(850161-08-9)
EPA Substance Registry System: (4RS)-3-(tert-butoxy)-4-hydroxy-2-methyl-4-{(3R,6S)-6-methyl-3-[(2S,4E)-2-methyl-4,6-heptadien-2-yl]-1-cyclohexenyl}-2-cyclobuten-1-one(850161-08-9)

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HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 850161-08-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 850161-08-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,5,0,1,6 and 1 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 850161-08:
(8*8)+(7*5)+(6*0)+(5*1)+(4*6)+(3*1)+(2*0)+(1*8)=139
139 % 10 = 9
So 850161-08-9 is a valid CAS Registry Number.

850161-08-9Upstream product

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850161-08-9Relevant academic research and scientific papers

Total synthesis of (-)-colombiasin A and (-)-elisapterosin B

Harrowven, David C.,Pascoe, David D.,Demurtas, Daniela,Bourne, Heather O.

, p. 1221 - 1222 (2007/10/03)

Intramolecular cycloaddition reactions are central in the total syntheses of colombiasin A (1) and elisapterosin B (2) described, which use (-)-dihydrocarvone as the starting material. A Moore rearrangement of a vinylcyclobutene is used to initiate the cycloaddition.

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