Cas 1147280-01-0,1-(4-bromophenyl)-N-cyclohexyl-6,7-dimethoxy-3,4-dihydroisoquinolin-2(1H)-carboxamide

1147280-01-0

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Basic information

Product Name: 1-(4-bromophenyl)-N-cyclohexyl-6,7-dimethoxy-3,4-dihydroisoquinolin-2(1H)-carboxamide
Synonyms: 1-(4-bromophenyl)-N-cyclohexyl-6,7-dimethoxy-3,4-dihydroisoquinolin-2(1H)-carboxamide
CAS NO:1147280-01-0
Molecular Formula:
Molecular Weight: 473.41
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-cyclohexyl-6,7-dimethoxy-3,4-dihydroisoquinolin-2(1H)-carboxamide(CAS DataBase Reference)
NIST Chemistry Reference: 1-(4-bromophenyl)-N-cyclohexyl-6,7-dimethoxy-3,4-dihydroisoquinolin-2(1H)-carboxamide(1147280-01-0)
EPA Substance Registry System: 1-(4-bromophenyl)-N-cyclohexyl-6,7-dimethoxy-3,4-dihydroisoquinolin-2(1H)-carboxamide(1147280-01-0)

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: 1147280-01-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1147280-01-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,4,7,2,8 and 0 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1147280-01:
(9*1)+(8*1)+(7*4)+(6*7)+(5*2)+(4*8)+(3*0)+(2*0)+(1*1)=130
130 % 10 = 0
So 1147280-01-0 is a valid CAS Registry Number.

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1147280-01-0Relevant 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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