Cas 60769-96-2,(5R*)-4-benzoyl-1,5-dihydro-3-hydroxy-5-(2-oxocyclopentyl)-2H-pyrrol-2-one

60769-96-2

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Basic information

Product Name: (5R*)-4-benzoyl-1,5-dihydro-3-hydroxy-5-(2-oxocyclopentyl)-2H-pyrrol-2-one
Synonyms: (5R*)-4-benzoyl-1,5-dihydro-3-hydroxy-5-(2-oxocyclopentyl)-2H-pyrrol-2-one
CAS NO:60769-96-2
Molecular Formula:
Molecular Weight: 433.461
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: (5R*)-4-benzoyl-1,5-dihydro-3-hydroxy-5-(2-oxocyclopentyl)-2H-pyrrol-2-one(CAS DataBase Reference)
NIST Chemistry Reference: (5R*)-4-benzoyl-1,5-dihydro-3-hydroxy-5-(2-oxocyclopentyl)-2H-pyrrol-2-one(60769-96-2)
EPA Substance Registry System: (5R*)-4-benzoyl-1,5-dihydro-3-hydroxy-5-(2-oxocyclopentyl)-2H-pyrrol-2-one(60769-96-2)

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: 60769-96-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 60769-96-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,7,6 and 9 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 60769-96:
(7*6)+(6*0)+(5*7)+(4*6)+(3*9)+(2*9)+(1*6)=152
152 % 10 = 2
So 60769-96-2 is a valid CAS Registry Number.

60769-96-2Upstream product

60769-96-2Downstream Products

60769-96-2Relevant academic research and scientific papers

Dioxopyrrolines. LX. Cycloaddition reaction of 4-benzoyl-5- ethoxycarbonyl-1-phenyl-1H-pyrrole-2,3-dione to olefins: An inverse-electron- demand hetero Diels-Alder reaction

Horiguchi,Sano,Tsuda

, p. 670 - 674 (2007/10/03)

Thermal cycloaddition of 4-benzoyl-5-ethoxycarbonyl-1-phenyl-1H-pyrrole- 2,3-dione (dioxopyrroline) 1 to electron-rich olefins smoothly proceeded in a highly regio- and stereoselective manner to give pyranopyrrole derivatives in excellent yields. The reac

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