Cas 634151-26-1,2(1H)-Isoquinolinecarboxylic acid, 1-[(2-bromophenyl)methyl]-3,4-dihydro-7-hydroxy-6-methoxy-, methyl ester

634151-26-1

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Basic information

Product Name: 2(1H)-Isoquinolinecarboxylic acid, 1-[(2-bromophenyl)methyl]-3,4-dihydro-7-hydroxy-6-methoxy-, methyl ester
Synonyms:
CAS NO:634151-26-1
Molecular Formula: C19H20BrNO4
Molecular Weight: 406.276
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: 2(1H)-Isoquinolinecarboxylic acid, 1-[(2-bromophenyl)methyl]-3,4-dihydro-7-hydroxy-6-methoxy-, methyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 2(1H)-Isoquinolinecarboxylic acid, 1-[(2-bromophenyl)methyl]-3,4-dihydro-7-hydroxy-6-methoxy-, methyl ester(634151-26-1)
EPA Substance Registry System: 2(1H)-Isoquinolinecarboxylic acid, 1-[(2-bromophenyl)methyl]-3,4-dihydro-7-hydroxy-6-methoxy-, methyl ester(634151-26-1)

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: 634151-26-1(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 634151-26-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,3,4,1,5 and 1 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 634151-26:
(8*6)+(7*3)+(6*4)+(5*1)+(4*5)+(3*1)+(2*2)+(1*6)=131
131 % 10 = 1
So 634151-26-1 is a valid CAS Registry Number.

634151-26-1Upstream product

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634151-26-1Relevant academic research and scientific papers

Intramolecular ortho-arylation of phenols utilized in the synthesis of the aporphine alkaloids (±)-lirinidine and (±)-nuciferine

Cuny, Gregory D.

, p. 8149 - 8152 (2007/10/03)

A palladium-mediated intramolecular phenol ortho-arylation reaction applied to the construction of aporphine alkaloids is reported. Most significantly, the efficiency of this transformation was enhanced by the utilization of trialkylphosphine (i.e. tricyc

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