Cas 1432732-97-2,dimethyl 2-(benzo[d][1,3]dioxol-5-yl)-2-(4-methoxyphenyl)-5-oxo-2,5-dihydrofuran-3,4-dicarboxylate

1432732-97-2

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Basic information

Product Name: dimethyl 2-(benzo[d][1,3]dioxol-5-yl)-2-(4-methoxyphenyl)-5-oxo-2,5-dihydrofuran-3,4-dicarboxylate
Synonyms: dimethyl 2-(benzo[d][1,3]dioxol-5-yl)-2-(4-methoxyphenyl)-5-oxo-2,5-dihydrofuran-3,4-dicarboxylate
CAS NO:1432732-97-2
Molecular Formula:
Molecular Weight: 426.38
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: dimethyl 2-(benzo[d][1,3]dioxol-5-yl)-2-(4-methoxyphenyl)-5-oxo-2,5-dihydrofuran-3,4-dicarboxylate(CAS DataBase Reference)
NIST Chemistry Reference: dimethyl 2-(benzo[d][1,3]dioxol-5-yl)-2-(4-methoxyphenyl)-5-oxo-2,5-dihydrofuran-3,4-dicarboxylate(1432732-97-2)
EPA Substance Registry System: dimethyl 2-(benzo[d][1,3]dioxol-5-yl)-2-(4-methoxyphenyl)-5-oxo-2,5-dihydrofuran-3,4-dicarboxylate(1432732-97-2)

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: 1432732-97-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1432732-97-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,3,2,7,3 and 2 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1432732-97:
(9*1)+(8*4)+(7*3)+(6*2)+(5*7)+(4*3)+(3*2)+(2*9)+(1*7)=152
152 % 10 = 2
So 1432732-97-2 is a valid CAS Registry Number.

1432732-97-2Upstream product

496-14-0 1,3-dihydroisobenzofuran

1432732-97-2Downstream Products

1432732-97-2Relevant academic research and scientific papers

A mild approach to diarylfuranones via functionalized 2-arylfurans

Dellagreca, Marina,Zuppolini, Simona,Zarrelli, Armando,Iesce, Maria R.,Previtera, Lucio

, p. 4725 - 4730 (2013)

5,5- and 3,5-Diarylfuranones have been obtained in a three-step one-pot manner. The procedure starts from photooxygenation of easily accessible arylfurans followed by in situ base treatment and finally by triflic anhydride mediated acylation of activated

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