Cas 82652-61-7,(4aR,5R,8aR)-6-Formyl-1,4a-dimethyl-5-(4-methyl-3-oxo-pentyl)-1,2,3,4,4a,5,8,8a-octahydro-naphthalene-1-carboxylic acid methyl ester

82652-61-7

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Basic information

Product Name: (4aR,5R,8aR)-6-Formyl-1,4a-dimethyl-5-(4-methyl-3-oxo-pentyl)-1,2,3,4,4a,5,8,8a-octahydro-naphthalene-1-carboxylic acid methyl ester
Synonyms: (4aR,5R,8aR)-6-Formyl-1,4a-dimethyl-5-(4-methyl-3-oxo-pentyl)-1,2,3,4,4a,5,8,8a-octahydro-naphthalene-1-carboxylic acid methyl ester
CAS NO:82652-61-7
Molecular Formula:
Molecular Weight: 348.483
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: (4aR,5R,8aR)-6-Formyl-1,4a-dimethyl-5-(4-methyl-3-oxo-pentyl)-1,2,3,4,4a,5,8,8a-octahydro-naphthalene-1-carboxylic acid methyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (4aR,5R,8aR)-6-Formyl-1,4a-dimethyl-5-(4-methyl-3-oxo-pentyl)-1,2,3,4,4a,5,8,8a-octahydro-naphthalene-1-carboxylic acid methyl ester(82652-61-7)
EPA Substance Registry System: (4aR,5R,8aR)-6-Formyl-1,4a-dimethyl-5-(4-methyl-3-oxo-pentyl)-1,2,3,4,4a,5,8,8a-octahydro-naphthalene-1-carboxylic acid methyl ester(82652-61-7)

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: 82652-61-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 82652-61-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,2,6,5 and 2 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 82652-61:
(7*8)+(6*2)+(5*6)+(4*5)+(3*2)+(2*6)+(1*1)=137
137 % 10 = 7
So 82652-61-7 is a valid CAS Registry Number.

82652-61-7Upstream product

22552-63-2 methyl 13β,14β-dihydroxyabieta-7-en-18-oate

82652-61-7Downstream Products

82652-61-7Relevant academic research and scientific papers

Regioselective routes towards 14-hydroxyabietane diterpenes. A formal synthesis of immunosuppressant (-)-triptolide from (+)-abietic acid

Alvarez-Manzaneda, Enrique,Chahboun, Rachid,Bentaleb, Faouzia,Alvarez, Esteban,Escobar, M. Angeles,Sad-Diki, Said,Cano, Maria José,Messouri, Ibtissam

, p. 11204 - 11212 (2007)

Two procedures to introduce an oxygenated function into the C-14 of abietane diterpenes with complete regioselectivity have been developed. Utilizing these, the synthesis of the antileishmanial quinone (-)-12-deoxyroyleanone (1) and a formal synthesis of antitumour and immunosuppressant (-)-triptonide (7) and (-)-triptolide (8) from (+)-abietic acid (13) have been carried out.

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