Cas 924263-25-2,Propanedioic acid, 2-[(2E)-3-(4-methylphenyl)-2-propen-1-yl]-2-(2-propen-1-yl)-, 1,3-dimethyl ester

924263-25-2

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Basic information

Product Name: Propanedioic acid, 2-[(2E)-3-(4-methylphenyl)-2-propen-1-yl]-2-(2-propen-1-yl)-, 1,3-dimethyl ester
Synonyms:
CAS NO:924263-25-2
Molecular Formula: C18H22O4
Molecular Weight: 302.37
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: Propanedioic acid, 2-[(2E)-3-(4-methylphenyl)-2-propen-1-yl]-2-(2-propen-1-yl)-, 1,3-dimethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: Propanedioic acid, 2-[(2E)-3-(4-methylphenyl)-2-propen-1-yl]-2-(2-propen-1-yl)-, 1,3-dimethyl ester(924263-25-2)
EPA Substance Registry System: Propanedioic acid, 2-[(2E)-3-(4-methylphenyl)-2-propen-1-yl]-2-(2-propen-1-yl)-, 1,3-dimethyl ester(924263-25-2)

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: 924263-25-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 924263-25-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,2,4,2,6 and 3 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 924263-25:
(8*9)+(7*2)+(6*4)+(5*2)+(4*6)+(3*3)+(2*2)+(1*5)=162
162 % 10 = 2
So 924263-25-2 is a valid CAS Registry Number.

924263-25-2Upstream product

924263-25-2Downstream Products

924263-25-2Relevant academic research and scientific papers

Mechanism of cycloisomerisation of 1,6-heptadienes catalysed by [(tBuCN)2PdCl2]: Remarkable influence of exogenous and endogenous 1,6- And 1,5-diene ligands

Bray, Katharine L.,Lloyd-Jones, Guy C.,Munoz, M. Paz,Slatford, Paul A.,Tan, Emily H. P.,Tyler-Mahon, Amanda R.,Worthington, Paul A.

, p. 8650 - 8663 (2006)

The mechanism of the highly regioselective cycloisomerisation of dimethyl hept-1,6-dienyl-4,4-dicarboxylate (1) by a neutral pre-catalyst, [(tBuCN) 2PdCl2] (8), to generate dimethyl 3,4-dimethylcyclopent-2- ene-1,1-dicarboxylate (3)

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