Cas 747383-68-2,E-3-(3-benzylamino-1-propen-1-yl)-2-ethoxycarbonyl-4-phenylquinoline

747383-68-2

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Basic information

Product Name: E-3-(3-benzylamino-1-propen-1-yl)-2-ethoxycarbonyl-4-phenylquinoline
Synonyms: E-3-(3-benzylamino-1-propen-1-yl)-2-ethoxycarbonyl-4-phenylquinoline
CAS NO:747383-68-2
Molecular Formula:
Molecular Weight: 422.527
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: E-3-(3-benzylamino-1-propen-1-yl)-2-ethoxycarbonyl-4-phenylquinoline(CAS DataBase Reference)
NIST Chemistry Reference: E-3-(3-benzylamino-1-propen-1-yl)-2-ethoxycarbonyl-4-phenylquinoline(747383-68-2)
EPA Substance Registry System: E-3-(3-benzylamino-1-propen-1-yl)-2-ethoxycarbonyl-4-phenylquinoline(747383-68-2)

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: 747383-68-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 747383-68-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,4,7,3,8 and 3 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 747383-68:
(8*7)+(7*4)+(6*7)+(5*3)+(4*8)+(3*3)+(2*6)+(1*8)=202
202 % 10 = 2
So 747383-68-2 is a valid CAS Registry Number.

747383-68-2Upstream product

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747383-68-2Relevant academic research and scientific papers

Synthesis of 4-Substituted 11-Phenyl-1,2,3,4-tetrahydro-5H-azepinoquinolin-5-one Derivatives as Potential Peripheral Benzodiazepine-Receptor Ligands

Cappelli, Andrea,Anzini, Maurizio,Vomero, Salvatore

, p. 1265 - 1272 (2007/10/02)

The synthesis of semirigid analogs of PK 11195, the highly specific peripheral benzodiazepine-receptor ligand, is reported.Compound (4) underwent the Wittig reaction with acetaldehyde to give olefin (7) which after allylic bromination was aminated to give

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