Cas 1147279-68-2,1-(4-bromophenyl)-N-isopropyl-6,7-dimethoxy-3,4-dihydroisoquinolin-2(1H)-carboxamide

1147279-68-2

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Basic information

Product Name: 1-(4-bromophenyl)-N-isopropyl-6,7-dimethoxy-3,4-dihydroisoquinolin-2(1H)-carboxamide
Synonyms: 1-(4-bromophenyl)-N-isopropyl-6,7-dimethoxy-3,4-dihydroisoquinolin-2(1H)-carboxamide
CAS NO:1147279-68-2
Molecular Formula:
Molecular Weight: 433.345
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: 1-(4-bromophenyl)-N-isopropyl-6,7-dimethoxy-3,4-dihydroisoquinolin-2(1H)-carboxamide(CAS DataBase Reference)
NIST Chemistry Reference: 1-(4-bromophenyl)-N-isopropyl-6,7-dimethoxy-3,4-dihydroisoquinolin-2(1H)-carboxamide(1147279-68-2)
EPA Substance Registry System: 1-(4-bromophenyl)-N-isopropyl-6,7-dimethoxy-3,4-dihydroisoquinolin-2(1H)-carboxamide(1147279-68-2)

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: 1147279-68-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1147279-68-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,4,7,2,7 and 9 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1147279-68:
(9*1)+(8*1)+(7*4)+(6*7)+(5*2)+(4*7)+(3*9)+(2*6)+(1*8)=172
172 % 10 = 2
So 1147279-68-2 is a valid CAS Registry Number.

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1147279-68-2Relevant 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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