Cas 125041-77-2,8-Eth-(Z)-ylidene-4,4,6-trimethyl-2-oxo-bicyclo[4.2.0]octane-7-carboxylic acid ethyl ester

125041-77-2

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Basic information

Product Name: 8-Eth-(Z)-ylidene-4,4,6-trimethyl-2-oxo-bicyclo[4.2.0]octane-7-carboxylic acid ethyl ester
Synonyms:
CAS NO:125041-77-2
Molecular Formula:
Molecular Weight: 264.365
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: 8-Eth-(Z)-ylidene-4,4,6-trimethyl-2-oxo-bicyclo[4.2.0]octane-7-carboxylic acid ethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 8-Eth-(Z)-ylidene-4,4,6-trimethyl-2-oxo-bicyclo[4.2.0]octane-7-carboxylic acid ethyl ester(125041-77-2)
EPA Substance Registry System: 8-Eth-(Z)-ylidene-4,4,6-trimethyl-2-oxo-bicyclo[4.2.0]octane-7-carboxylic acid ethyl ester(125041-77-2)

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: 125041-77-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 125041-77-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,5,0,4 and 1 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 125041-77:
(8*1)+(7*2)+(6*5)+(5*0)+(4*4)+(3*1)+(2*7)+(1*7)=92
92 % 10 = 2
So 125041-77-2 is a valid CAS Registry Number.

125041-77-2Upstream product

125041-77-2Downstream Products

125041-77-2Relevant academic research and scientific papers

UV irradiation of isophorone in presence of allenic esters

Gandhi, R. P.,Ishar, M. P. S.

, p. 381 - 384 (2007/10/02)

Irradiation of a mixture of isophorone and ethyl penta-2,3-dienoate (1a) or ethyl hexa-2,3-dienoate (1b) or ethyl 4-methyl-hexa-2,3-dienoate (1c) in methanol leads to novel addition compounds (2a-c) as major products and cyclobutane-adducts (3a-c) and (4a,b) as minor products.A mechanistic rationale for formation of 2a-c (E geometry around 3,4-double bond) is proffered.

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