Cas 1432504-78-3,7-(3,3-dimethylbut-1-ynyl)-2-(4-methoxyphenyl)-2-methyl-2,3-dihydrobenzofuran-5-ol

1432504-78-3

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Basic information

Product Name: 7-(3,3-dimethylbut-1-ynyl)-2-(4-methoxyphenyl)-2-methyl-2,3-dihydrobenzofuran-5-ol
Synonyms: 7-(3,3-dimethylbut-1-ynyl)-2-(4-methoxyphenyl)-2-methyl-2,3-dihydrobenzofuran-5-ol
CAS NO:1432504-78-3
Molecular Formula:
Molecular Weight: 336.431
EINECS: N/A
Product Categories: N/A
Mol File: 1432504-78-3.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: 7-(3,3-dimethylbut-1-ynyl)-2-(4-methoxyphenyl)-2-methyl-2,3-dihydrobenzofuran-5-ol(CAS DataBase Reference)
NIST Chemistry Reference: 7-(3,3-dimethylbut-1-ynyl)-2-(4-methoxyphenyl)-2-methyl-2,3-dihydrobenzofuran-5-ol(1432504-78-3)
EPA Substance Registry System: 7-(3,3-dimethylbut-1-ynyl)-2-(4-methoxyphenyl)-2-methyl-2,3-dihydrobenzofuran-5-ol(1432504-78-3)

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: 1432504-78-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1432504-78-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,3,2,5,0 and 4 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1432504-78:
(9*1)+(8*4)+(7*3)+(6*2)+(5*5)+(4*0)+(3*4)+(2*7)+(1*8)=133
133 % 10 = 3
So 1432504-78-3 is a valid CAS Registry Number.

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1432504-78-3Relevant articles and documents

Metal-controlled cycloaddition of 2-alkynyl-1,4-benzoquinones and styrenyl systems: Lewis acid versus π acid

Zhang, Li,Li, Zhiming,Fan, Renhua

supporting information, p. 2482 - 2485 (2013/06/27)

Metal-controlled cycloaddition of 2-alkynyl-1,4-benzoquinones and electron-rich styrenyl systems were investigated. The density functional theory (DFT) calculations revealed that the regioselectivity of the cycloaddition results from the different activat

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