Cas 136579-75-4,3-Methoxy-1,5-diphenyl-2,6,7-trioxa-bicyclo[3.2.0]hept-3-ene-4-carboxylic acid ethyl ester

136579-75-4

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Basic information

Product Name: 3-Methoxy-1,5-diphenyl-2,6,7-trioxa-bicyclo[3.2.0]hept-3-ene-4-carboxylic acid ethyl ester
Synonyms:
CAS NO:136579-75-4
Molecular Formula:
Molecular Weight: 354.359
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: 3-Methoxy-1,5-diphenyl-2,6,7-trioxa-bicyclo[3.2.0]hept-3-ene-4-carboxylic acid ethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 3-Methoxy-1,5-diphenyl-2,6,7-trioxa-bicyclo[3.2.0]hept-3-ene-4-carboxylic acid ethyl ester(136579-75-4)
EPA Substance Registry System: 3-Methoxy-1,5-diphenyl-2,6,7-trioxa-bicyclo[3.2.0]hept-3-ene-4-carboxylic acid ethyl ester(136579-75-4)

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: 136579-75-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 136579-75-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,6,5,7 and 9 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 136579-75:
(8*1)+(7*3)+(6*6)+(5*5)+(4*7)+(3*9)+(2*7)+(1*5)=164
164 % 10 = 4
So 136579-75-4 is a valid CAS Registry Number.

136579-75-4Upstream product

136579-75-4Downstream Products

136579-80-1 2-[2-Oxo-1,2-diphenyl-eth-(E)-ylidene]-malonic acid ethyl ester methyl ester

136579-75-4Relevant academic research and scientific papers

A Further Selective Pathway in Thermal Conversion of 2,5-Epidioxy-2-alkoxy-2,5-dihydrofurans (2-Alkoxyfuran endo-Peroxides). Synthesis of the First 5-Hydroperoxyfuran-2(5H)-ones

Iesce, M. Rosaria,Graziano, M. Liliana,Cermola, Flavio,Scarpati, Rachele

, p. 1061 - 1062 (2007/10/02)

Thermal conversion of the epidioxydihydrofurans 1 leads, via dioxyetanes 3, to the stereoisomeric dimers 4 which have a structural relationship with antitumor cyclic peroxides and represent convenient starting materials for several multifunctional compoun

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