Cas 141077-85-2,Cyclohexanecarboxylic acid, 1-[3-(acetyloxy)-2-methyl-2-propenyl]-5-methylene-2-oxo-, methyl ester

141077-85-2

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Basic information

Product Name: Cyclohexanecarboxylic acid, 1-[3-(acetyloxy)-2-methyl-2-propenyl]-5-methylene-2-oxo-, methyl ester
Synonyms:
CAS NO:141077-85-2
Molecular Formula: C15H20O5
Molecular Weight: 280.321
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: Cyclohexanecarboxylic acid, 1-[3-(acetyloxy)-2-methyl-2-propenyl]-5-methylene-2-oxo-, methyl ester(CAS DataBase Reference)
NIST Chemistry Reference: Cyclohexanecarboxylic acid, 1-[3-(acetyloxy)-2-methyl-2-propenyl]-5-methylene-2-oxo-, methyl ester(141077-85-2)
EPA Substance Registry System: Cyclohexanecarboxylic acid, 1-[3-(acetyloxy)-2-methyl-2-propenyl]-5-methylene-2-oxo-, methyl ester(141077-85-2)

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: 141077-85-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 141077-85-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,1,0,7 and 7 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 141077-85:
(8*1)+(7*4)+(6*1)+(5*0)+(4*7)+(3*7)+(2*8)+(1*5)=112
112 % 10 = 2
So 141077-85-2 is a valid CAS Registry Number.

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141077-85-2Relevant academic research and scientific papers

On the palladium catalyzed reaction of methallyl-1,1-diacetate with cyclic β-ketoesters. Intervention of hidden mechanisms

Gravel,Benoit,Kumanovic,Sivaramakrishnan

, p. 1403 - 1406 (2007/10/02)

Palladium(O) catalysis in the title reaction causes the release of methacrolein which competes effectively with the π-allyl species in product formation, a bicycloannulated derivative, when DBU is used as base.

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