Cas 796097-51-3,N-tert-butyl-6,7-dimethoxy-1-phenyl-3,4-dihydroisoquinolin-2(1H)-carboxamide

796097-51-3

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Basic information

Product Name: N-tert-butyl-6,7-dimethoxy-1-phenyl-3,4-dihydroisoquinolin-2(1H)-carboxamide
Synonyms: N-tert-butyl-6,7-dimethoxy-1-phenyl-3,4-dihydroisoquinolin-2(1H)-carboxamide
CAS NO:796097-51-3
Molecular Formula:
Molecular Weight: 368.476
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: N-tert-butyl-6,7-dimethoxy-1-phenyl-3,4-dihydroisoquinolin-2(1H)-carboxamide(CAS DataBase Reference)
NIST Chemistry Reference: N-tert-butyl-6,7-dimethoxy-1-phenyl-3,4-dihydroisoquinolin-2(1H)-carboxamide(796097-51-3)
EPA Substance Registry System: N-tert-butyl-6,7-dimethoxy-1-phenyl-3,4-dihydroisoquinolin-2(1H)-carboxamide(796097-51-3)

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: 796097-51-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 796097-51-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,9,6,0,9 and 7 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 796097-51:
(8*7)+(7*9)+(6*6)+(5*0)+(4*9)+(3*7)+(2*5)+(1*1)=223
223 % 10 = 3
So 796097-51-3 is a valid CAS Registry Number.

796097-51-3Upstream product

796097-51-3Downstream Products

796097-51-3Relevant academic research and scientific papers

Solution-phase parallel synthesis and evaluation of anticonvulsant activity of N-substituted-3,4-dihydroisoquinoline-2(1H)-carboxamides

Gitto, Rosaria,Pagano, Benedetta,Citraro, Rita,Scicchitano, Francesca,De Sarro, Giovanbattista,Chimirri, Alba

experimental part, p. 1349 - 1354 (2009/09/27)

In our previous studies we identified several isoquinoline derivatives displaying potent anticonvulsant effects in different animal models of epilepsy. With the aim to exploit the main structure-activity relationships (SAR) for this class of compounds we

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