Cas 125593-57-9,(4,4-Dimethoxy-1-phenyl-cyclohexa-2,5-dienyl)-carbamic acid tert-butyl ester

125593-57-9

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Basic information

Product Name: (4,4-Dimethoxy-1-phenyl-cyclohexa-2,5-dienyl)-carbamic acid tert-butyl ester
Synonyms: (4,4-Dimethoxy-1-phenyl-cyclohexa-2,5-dienyl)-carbamic acid tert-butyl ester
CAS NO:125593-57-9
Molecular Formula:
Molecular Weight: 331.412
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: (4,4-Dimethoxy-1-phenyl-cyclohexa-2,5-dienyl)-carbamic acid tert-butyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (4,4-Dimethoxy-1-phenyl-cyclohexa-2,5-dienyl)-carbamic acid tert-butyl ester(125593-57-9)
EPA Substance Registry System: (4,4-Dimethoxy-1-phenyl-cyclohexa-2,5-dienyl)-carbamic acid tert-butyl ester(125593-57-9)

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: 125593-57-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 125593-57-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,5,5,9 and 3 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 125593-57:
(8*1)+(7*2)+(6*5)+(5*5)+(4*9)+(3*3)+(2*5)+(1*7)=139
139 % 10 = 9
So 125593-57-9 is a valid CAS Registry Number.

125593-57-9Upstream product

125593-57-9Downstream Products

125593-47-7 4--4-phenyl-2,5-cyclohexadienone

125593-57-9Relevant academic research and scientific papers

The Chemisty of Acylated Quinone Imine Ketals. Nucleophilic and Organolithium Addition Reactions

Swenton, John S.,Bonke, Brian R.,Clark, William M.,Chen, Chung-Pin,Martin, Kevin V.

, p. 2027 - 2034 (2007/10/02)

Acylated quinone imine ketals are readily available via anodic oxidation of p-methoxybenzanilides and p-methoxyacetanilides.These compounds react with a variety of nucleophiles to give the corresponding substituted 2- and/or 3-substituted-4-methoxyanilide

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