Cas 1321200-93-4,(3R,4R)-5-benzoyl-3-(3-fluorobenzyl)-4,6-diphenyl-3,4-dihydro-2H-pyran-2-one

1321200-93-4

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Basic information

Product Name: (3R,4R)-5-benzoyl-3-(3-fluorobenzyl)-4,6-diphenyl-3,4-dihydro-2H-pyran-2-one
Synonyms: (3R,4R)-5-benzoyl-3-(3-fluorobenzyl)-4,6-diphenyl-3,4-dihydro-2H-pyran-2-one
CAS NO:1321200-93-4
Molecular Formula:
Molecular Weight: 462.52
EINECS: N/A
Product Categories: N/A
Mol File: 1321200-93-4.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: (3R,4R)-5-benzoyl-3-(3-fluorobenzyl)-4,6-diphenyl-3,4-dihydro-2H-pyran-2-one(CAS DataBase Reference)
NIST Chemistry Reference: (3R,4R)-5-benzoyl-3-(3-fluorobenzyl)-4,6-diphenyl-3,4-dihydro-2H-pyran-2-one(1321200-93-4)
EPA Substance Registry System: (3R,4R)-5-benzoyl-3-(3-fluorobenzyl)-4,6-diphenyl-3,4-dihydro-2H-pyran-2-one(1321200-93-4)

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: 1321200-93-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1321200-93-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,2,1,2,0 and 0 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1321200-93:
(9*1)+(8*3)+(7*2)+(6*1)+(5*2)+(4*0)+(3*0)+(2*9)+(1*3)=84
84 % 10 = 4
So 1321200-93-4 is a valid CAS Registry Number.

1321200-93-4Upstream product

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1321200-93-4Relevant articles and documents

Enantioselective Diels-Alder reactions of enals and alkylidene diketones catalyzed by N-heterocyclic carbenes

Fang, Xinqiang,Chen, Xingkuan,Chi, Yonggui Robin

supporting information; experimental part, p. 4708 - 4711 (2011/10/18)

An electron-withdrawing group was introduced to the α-position of chalcones, and the resulting alkylidene diketones showed new reactivities with enals under the catalysis of N-heterocyclic carbenes (NHCs). Selective activation of enals affords enolate equ

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