Cas 85873-99-0,(4aS,10aR)-1-Benzoyloxymethyl-7-isopropyl-4a-methyl-3,4,4a,9,10,10a-hexahydro-phenanthrene-2-carboxylic acid methyl ester

85873-99-0

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Basic information

Product Name: (4aS,10aR)-1-Benzoyloxymethyl-7-isopropyl-4a-methyl-3,4,4a,9,10,10a-hexahydro-phenanthrene-2-carboxylic acid methyl ester
Synonyms:
CAS NO:85873-99-0
Molecular Formula:
Molecular Weight: 432.56
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: (4aS,10aR)-1-Benzoyloxymethyl-7-isopropyl-4a-methyl-3,4,4a,9,10,10a-hexahydro-phenanthrene-2-carboxylic acid methyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (4aS,10aR)-1-Benzoyloxymethyl-7-isopropyl-4a-methyl-3,4,4a,9,10,10a-hexahydro-phenanthrene-2-carboxylic acid methyl ester(85873-99-0)
EPA Substance Registry System: (4aS,10aR)-1-Benzoyloxymethyl-7-isopropyl-4a-methyl-3,4,4a,9,10,10a-hexahydro-phenanthrene-2-carboxylic acid methyl ester(85873-99-0)

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: 85873-99-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 85873-99-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,5,8,7 and 3 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 85873-99:
(7*8)+(6*5)+(5*8)+(4*7)+(3*3)+(2*9)+(1*9)=190
190 % 10 = 0
So 85873-99-0 is a valid CAS Registry Number.

85873-99-0Upstream product

94-36-0 dibenzoyl peroxide

85873-99-0Downstream Products

85873-99-0Relevant academic research and scientific papers

SYNTHESES OF THE A RING ANALOGS OF TRIPTOLIDE AND TRIPDIOLIDE

Tokoroyama, Takashi,Kondo, Akihiro,Ezaki, Yoichiro

, p. 203 - 206 (1983)

The synthesis of an A ring analog of tripdiolide as well as revised procedures for the synthesis of a triptolide analog (isodehydroabietenolide) from dehydroabietic acid via the previously reported intermediate is described.

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