Cas 170241-31-3,12-benzoyloxy-5,10-friedo-4,5-seco-abieta-5<sup>(10)</sup>,6,8,12-tetraene-3,11,14-trione

170241-31-3

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Basic information

Product Name: 12-benzoyloxy-5,10-friedo-4,5-seco-abieta-5⁽¹⁰⁾,6,8,12-tetraene-3,11,14-trione
Synonyms: 12-benzoyloxy-5,10-friedo-4,5-seco-abieta-5⁽¹⁰⁾,6,8,12-tetraene-3,11,14-trione
CAS NO:170241-31-3
Molecular Formula:
Molecular Weight: 432.516
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: 12-benzoyloxy-5,10-friedo-4,5-seco-abieta-5⁽¹⁰⁾,6,8,12-tetraene-3,11,14-trione(CAS DataBase Reference)
NIST Chemistry Reference: 12-benzoyloxy-5,10-friedo-4,5-seco-abieta-5⁽¹⁰⁾,6,8,12-tetraene-3,11,14-trione(170241-31-3)
EPA Substance Registry System: 12-benzoyloxy-5,10-friedo-4,5-seco-abieta-5⁽¹⁰⁾,6,8,12-tetraene-3,11,14-trione(170241-31-3)

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: 170241-31-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 170241-31-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,0,2,4 and 1 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 170241-31:
(8*1)+(7*7)+(6*0)+(5*2)+(4*4)+(3*1)+(2*3)+(1*1)=93
93 % 10 = 3
So 170241-31-3 is a valid CAS Registry Number.

170241-31-3Upstream product

170241-30-2 12-benzoyloxy-3-hydroxy-5,10-friedo-4,5-seco-abieta-5⁽¹⁰⁾,6,8,12-tetraene-11,14-dione

170241-31-3Downstream Products

119139-56-9 3-oxosapriparaquinone

170241-31-3Relevant academic research and scientific papers

Synthesis of 3-oxosapriparaquinone, a diterpene from Salvia prionitis hance

Matsumoto,Takeda,Soh,Matsumura,Imai

, p. 2705 - 2708 (1995)

12-Acetoxy-5,16-friedo-4,5-seco-abieta-3,5(10),6,8,11,13-hexaene prepared from (+)-dehydroabietic acid, was converted into a natural rearranged abietane-type diterpene, 3-oxosapriparaquinone, via 12-benzoyloxy-3-hydroxy-5,10-friedo-4,5-seco-abieta-5(10),6,8,12-tetra ene-11,14-dione by a series of reactions: hydroboration-oxidation, benzoyl peroxide oxidation, Jones oxidation, and alkaline hydrolysis.

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