Cas 1192179-77-3,3-(1,3-benzodioxol-5-yl)-2-(4-methoxycarbonylphenyl)-4H-furo[3,2-c][1]benzopyran-4-one

1192179-77-3

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Basic information

Product Name: 3-(1,3-benzodioxol-5-yl)-2-(4-methoxycarbonylphenyl)-4H-furo[3,2-c][1]benzopyran-4-one
Synonyms: 3-(1,3-benzodioxol-5-yl)-2-(4-methoxycarbonylphenyl)-4H-furo[3,2-c][1]benzopyran-4-one
CAS NO:1192179-77-3
Molecular Formula:
Molecular Weight: 440.409
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-(1,3-benzodioxol-5-yl)-2-(4-methoxycarbonylphenyl)-4H-furo[3,2-c][1]benzopyran-4-one(CAS DataBase Reference)
NIST Chemistry Reference: 3-(1,3-benzodioxol-5-yl)-2-(4-methoxycarbonylphenyl)-4H-furo[3,2-c][1]benzopyran-4-one(1192179-77-3)
EPA Substance Registry System: 3-(1,3-benzodioxol-5-yl)-2-(4-methoxycarbonylphenyl)-4H-furo[3,2-c][1]benzopyran-4-one(1192179-77-3)

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: 1192179-77-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1192179-77-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,9,2,1,7 and 9 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1192179-77:
(9*1)+(8*1)+(7*9)+(6*2)+(5*1)+(4*7)+(3*9)+(2*7)+(1*7)=173
173 % 10 = 3
So 1192179-77-3 is a valid CAS Registry Number.

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1192179-77-3Relevant academic research and scientific papers

A Pd-Catalyzed heteroannulation approach to 2,3-Disubstituted furo[3,2-c]coumarins

Raffa, Guillaume,Rusch, Marion,Balme, Genevieve,Monteiro, Nuno

supporting information; experimental part, p. 5254 - 5257 (2010/02/28)

The Pd-catalyzed cyclofunctionalization of 3-alkynyl-4-methoxycoumarins with aryl halides resulted in the selective formation of 3-arylfuro[3,2c] coumarins in lieu of the expected regioisomeric 3-arylfuro[2,3-b]chromones. A mechanism involving the linear

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