Cas 1451050-77-3,1-phenyl-2',3'-dihydro-1'H-spiro[pyrrolidine-3,4'-quinoline]-2,5-dione

1451050-77-3

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Basic information

Product Name: 1-phenyl-2',3'-dihydro-1'H-spiro[pyrrolidine-3,4'-quinoline]-2,5-dione
Synonyms:
CAS NO:1451050-77-3
Molecular Formula:
Molecular Weight: 292.337
EINECS: N/A
Product Categories: N/A
Mol File: 1451050-77-3.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: 1-phenyl-2',3'-dihydro-1'H-spiro[pyrrolidine-3,4'-quinoline]-2,5-dione(CAS DataBase Reference)
NIST Chemistry Reference: 1-phenyl-2',3'-dihydro-1'H-spiro[pyrrolidine-3,4'-quinoline]-2,5-dione(1451050-77-3)
EPA Substance Registry System: 1-phenyl-2',3'-dihydro-1'H-spiro[pyrrolidine-3,4'-quinoline]-2,5-dione(1451050-77-3)

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: 1451050-77-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1451050-77-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,5,1,0,5 and 0 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1451050-77:
(9*1)+(8*4)+(7*5)+(6*1)+(5*0)+(4*5)+(3*0)+(2*7)+(1*7)=123
123 % 10 = 3
So 1451050-77-3 is a valid CAS Registry Number.

1451050-77-3Upstream product

1451050-77-3Downstream Products

1451050-77-3Relevant articles and documents

Amphiphilic methyleneamino synthon through organic dye catalyzed- decarboxylative aminoalkylation

Chen, Li,Chao, Chin Sheng,Pan, Yuanhang,Dong, Sheng,Teo, Yew Chin,Wang, Jian,Tan, Choon-Hong

, p. 5922 - 5925 (2013)

The utilization of a photo-induced synthon generated from N-phenyl glycine by an organic dye and visible light irradiation is disclosed. The intermediate could be coupled with either a radical or a nucleophile in a simple operation to afford several natural product-like compounds.

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