Cas 312536-76-8,2,2-dimethyl-4,8-dioxo-5-phenyl-1,3,4,5,7,8,9,10,11,12-decahydro-2H-[1]benzothieno[3',2':5,6]pyrimido[1,2-a]quinoline-6-carbonitrile

312536-76-8

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Basic information

Product Name: 2,2-dimethyl-4,8-dioxo-5-phenyl-1,3,4,5,7,8,9,10,11,12-decahydro-2H-[1]benzothieno[3',2':5,6]pyrimido[1,2-a]quinoline-6-carbonitrile
Synonyms: 2,2-dimethyl-4,8-dioxo-5-phenyl-1,3,4,5,7,8,9,10,11,12-decahydro-2H-[1]benzothieno[3',2':5,6]pyrimido[1,2-a]quinoline-6-carbonitrile
CAS NO:312536-76-8
Molecular Formula: C27H25N3O2S
Molecular Weight: 455.5713
EINECS: N/A
Product Categories: N/A
Mol File: 312536-76-8.mol

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: /
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: 2,2-dimethyl-4,8-dioxo-5-phenyl-1,3,4,5,7,8,9,10,11,12-decahydro-2H-[1]benzothieno[3',2':5,6]pyrimido[1,2-a]quinoline-6-carbonitrile(CAS DataBase Reference)
NIST Chemistry Reference: 2,2-dimethyl-4,8-dioxo-5-phenyl-1,3,4,5,7,8,9,10,11,12-decahydro-2H-[1]benzothieno[3',2':5,6]pyrimido[1,2-a]quinoline-6-carbonitrile(312536-76-8)
EPA Substance Registry System: 2,2-dimethyl-4,8-dioxo-5-phenyl-1,3,4,5,7,8,9,10,11,12-decahydro-2H-[1]benzothieno[3',2':5,6]pyrimido[1,2-a]quinoline-6-carbonitrile(312536-76-8)

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: 312536-76-8(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 312536-76-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,1,2,5,3 and 6 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 312536-76:
(8*3)+(7*1)+(6*2)+(5*5)+(4*3)+(3*6)+(2*7)+(1*6)=118
118 % 10 = 8
So 312536-76-8 is a valid CAS Registry Number.

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312536-76-8Relevant academic research and scientific papers

Regioorientation in the Addition Reaction of α-Substituted Cinnamonitrile to Enamines Utilizing Chitosan as a Green Catalyst: Unambiguous Structural Characterization Using 2D-HMBC NMR Spectroscopy

Ghozlan, Said A. S.,Ahmed, Ahmed Gamal,Abdelhamid, Ismail Abdelshafy

, p. 817 - 823 (2016)

Hexahydroquinolines and their fused derivatives are obtained in good to excellent yields by proceeding through a simple, mild, and efficient procedure including the reaction of enamines with substituted cinnamonitriles using DABCO, piperidine, or chitosan

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