Cas 1334472-97-7,2-(2-([1,1'-biphenyl]-4-yl)-2-oxoethyl)-2-methylnaphtho[2,1-b]furan-1(2H)-one

1334472-97-7

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Basic information

Product Name: 2-(2-([1,1'-biphenyl]-4-yl)-2-oxoethyl)-2-methylnaphtho[2,1-b]furan-1(2H)-one
Synonyms: 2-(2-([1,1'-biphenyl]-4-yl)-2-oxoethyl)-2-methylnaphtho[2,1-b]furan-1(2H)-one
CAS NO:1334472-97-7
Molecular Formula:
Molecular Weight: 392.454
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: 2-(2-([1,1'-biphenyl]-4-yl)-2-oxoethyl)-2-methylnaphtho[2,1-b]furan-1(2H)-one(CAS DataBase Reference)
NIST Chemistry Reference: 2-(2-([1,1'-biphenyl]-4-yl)-2-oxoethyl)-2-methylnaphtho[2,1-b]furan-1(2H)-one(1334472-97-7)
EPA Substance Registry System: 2-(2-([1,1'-biphenyl]-4-yl)-2-oxoethyl)-2-methylnaphtho[2,1-b]furan-1(2H)-one(1334472-97-7)

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: 1334472-97-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1334472-97-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,3,4,4,7 and 2 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1334472-97:
(9*1)+(8*3)+(7*3)+(6*4)+(5*4)+(4*7)+(3*2)+(2*9)+(1*7)=157
157 % 10 = 7
So 1334472-97-7 is a valid CAS Registry Number.

1334472-97-7Upstream product

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1334472-97-7Relevant academic research and scientific papers

Efficient synthesis of benzofuranones: N-heterocyclic carbene (NHC)/base-catalyzed hydroacylation-stetter-rearrangement cascade

Padmanaban, Mohan,Biju, Akkattu T.,Glorius, Frank

, p. 5624 - 5627 (2011/12/03)

A N-heterocyclic carbene/base-catalyzed cascade reaction leading to the formation of functionalized benzofuranones is reported. The reaction proceeds via an intramolecular hydroacylation of unactivated alkynes followed by an intermolecular Stetter reactio

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