Cas 80371-11-5,(1R,4aR,4bR,7S,8S,9aS,10S,10aR)-2,8-dibenzoyloxy-4a-hydroxy-1,7-dimethylgibbane-1,10-dicarboxylic acid 1,4a-lactone methyl ester

80371-11-5

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Basic information

Product Name: (1R,4aR,4bR,7S,8S,9aS,10S,10aR)-2,8-dibenzoyloxy-4a-hydroxy-1,7-dimethylgibbane-1,10-dicarboxylic acid 1,4a-lactone methyl ester
Synonyms:
CAS NO:80371-11-5
Molecular Formula:
Molecular Weight: 572.655
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,4aR,4bR,7S,8S,9aS,10S,10aR)-2,8-dibenzoyloxy-4a-hydroxy-1,7-dimethylgibbane-1,10-dicarboxylic acid 1,4a-lactone methyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (1R,4aR,4bR,7S,8S,9aS,10S,10aR)-2,8-dibenzoyloxy-4a-hydroxy-1,7-dimethylgibbane-1,10-dicarboxylic acid 1,4a-lactone methyl ester(80371-11-5)
EPA Substance Registry System: (1R,4aR,4bR,7S,8S,9aS,10S,10aR)-2,8-dibenzoyloxy-4a-hydroxy-1,7-dimethylgibbane-1,10-dicarboxylic acid 1,4a-lactone methyl ester(80371-11-5)

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: 80371-11-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 80371-11-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,0,3,7 and 1 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 80371-11:
(7*8)+(6*0)+(5*3)+(4*7)+(3*1)+(2*1)+(1*1)=105
105 % 10 = 5
So 80371-11-5 is a valid CAS Registry Number.

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80371-11-5Relevant academic research and scientific papers

Studies on Gibberellin Synthesis. Assembly of an Ethanophenanthrenoid Lactone and Conversion into a Gibbane Derivative

Mander, Lewis N.,Pyne, Stephen G.

, p. 1899 - 1911 (2007/10/02)

Diazoketone (13), prepared by standard methods from 5-formyl-8-methoxy-1,2,3,4-tetrahydronaphthalene-2-carboxylic acid (7), was cyclized in trifluoroacetic acid to dienone (1) which underwent intramolecular 1,4-conjugate addition to afford the ethanophena

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