Cas 1260510-93-7,2-methyl-4,5-diphenyl-3-(phenyl((tetrahydrofuran-2-yl)methoxy)methyl)furan

1260510-93-7

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Basic information

Product Name: 2-methyl-4,5-diphenyl-3-(phenyl((tetrahydrofuran-2-yl)methoxy)methyl)furan
Synonyms: 2-methyl-4,5-diphenyl-3-(phenyl((tetrahydrofuran-2-yl)methoxy)methyl)furan
CAS NO:1260510-93-7
Molecular Formula:
Molecular Weight: 424.54
EINECS: N/A
Product Categories: N/A
Mol File: 1260510-93-7.mol
Article Data: 1

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: 2-methyl-4,5-diphenyl-3-(phenyl((tetrahydrofuran-2-yl)methoxy)methyl)furan(CAS DataBase Reference)
NIST Chemistry Reference: 2-methyl-4,5-diphenyl-3-(phenyl((tetrahydrofuran-2-yl)methoxy)methyl)furan(1260510-93-7)
EPA Substance Registry System: 2-methyl-4,5-diphenyl-3-(phenyl((tetrahydrofuran-2-yl)methoxy)methyl)furan(1260510-93-7)

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: 1260510-93-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1260510-93-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,6,0,5,1 and 0 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1260510-93:
(9*1)+(8*2)+(7*6)+(6*0)+(5*5)+(4*1)+(3*0)+(2*9)+(1*3)=117
117 % 10 = 7
So 1260510-93-7 is a valid CAS Registry Number.

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1260510-93-7Relevant articles and documents

Tetrasubstituted furans by PdII/CuI-cocatalyzed three-component domino reactions of 2-(1-alkynyl)-2-alken-1-ones, nucleophiles and diaryliodonium salts

Li, Wenbo,Zhang, Junliang

supporting information; experimental part, p. 8839 - 8841 (2011/02/21)

A novel Pd(OAc)2/CuI-cocatalyzed three-component reaction of 2-(1-alkynyl)-2-alken-1-ones, nucleophiles and diaryliodonium salts has been developed. The procedure allows the synthesis of tetrasubstituted furans in good to high yields under mild

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