123190-18-1

Basic information

• Product Name: 2(1H)-Isoquinolinecarboxylic acid, 1-[(2-bromo-4,5-dimethoxyphenyl)methyl]-7-[(ethoxycarbonyl)oxy]-3,4-dihydro-6-methoxy-, ethyl ester
• Synonyms: 2(1H)-Isoquinolinecarboxylic acid, 1-[(2-bromo-4,5-dimethoxyphenyl)methyl]-7-[(ethoxycarbonyl)oxy]-3,4-dihydro-6-methoxy-, ethyl ester
• CAS NO: 123190-18-1
• Molecular Formula: C₂₅H₃₀BrNO₈
• Molecular Weight: 0
• Mol File: 123190-18-1.mol
• Article Data: 1

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2(1H)-Isoquinolinecarboxylic acid, 1-[(2-bromo-4,5-dimethoxyphenyl)methyl]-7-[(ethoxycarbonyl)oxy]-3,4-dihydro-6-methoxy-, ethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: 2(1H)-Isoquinolinecarboxylic acid, 1-[(2-bromo-4,5-dimethoxyphenyl)methyl]-7-[(ethoxycarbonyl)oxy]-3,4-dihydro-6-methoxy-, ethyl ester(123190-18-1)
• EPA Substance Registry System: 2(1H)-Isoquinolinecarboxylic acid, 1-[(2-bromo-4,5-dimethoxyphenyl)methyl]-7-[(ethoxycarbonyl)oxy]-3,4-dihydro-6-methoxy-, ethyl ester(123190-18-1)

Safety Data

• Hazardous Substances Data: 123190-18-1(Hazardous Substances Data)

Usage

Molecular structure

2(1H)-Isoquinolinecarboxylic acid, 1-[(2-bromo-4,5-dimethoxyphenyl)methyl]-7-[(ethoxycarbonyl)oxy]-3,4-dihydro-6-methoxy-, ethyl ester is an organic compound with a complex structure, containing various functional groups.

Ester derivative

It is an ester derivative of isoquinolinecarboxylic acid, which means it has an ester functional group (-COO-) attached to the isoquinoline ring.

Bromo-dimethoxyphenylmethyl group

The compound contains a 2-bromo-4,5-dimethoxyphenylmethyl group, which is a substituted phenyl ring with a bromine atom at the 2-position and two methoxy groups at the 4and 5-positions.

Ethoxycarbonyl group

The compound also has an ethoxycarbonyl (-COOCH3) group, which is an ester functional group with an ethoxy (-OCH2CH3) substituent.

Methoxy group

It contains a methoxy (-OCH3) group, which is a methyl group attached to an oxygen atom.

Ethyl ester

The compound is classified as an ethyl ester, indicating that the ester functional group is derived from ethanol (C2H5OH).

Biological activity

The structure of the compound suggests potential biological activity or industrial applications, although further research and testing would be needed to determine its specific uses and properties.

Synthesis of other chemicals or pharmaceuticals

Due to its complex structure and various functional groups, the compound may be used in the synthesis of other chemicals or pharmaceuticals, but additional research is required to confirm its applications.

Upstream product

• 47706-26-3 7-benzyloxy-1-(2-bromo-4,5-dimethoxybenzyl)-1,2,3,4-tetrahydro-6-methoxyisoquinoline 
• 541-41-3 chloroformic acid ethyl ester 
• 120566-97-4 1-<2'-bromo-4',5'-dimethoxy>-7-hydroxy-6-methoxy-1,2,3,4-tetrahydroisoquinoline 

Downstream Products

• 51015-09-9 1-(2-bromo-4,5-dimethoxybenzyl)-2-ethoxycarbonyl-1,2,3,4-tetrahydro-7-hydroxy-6-methoxyisoquinoline 

Relevant articles and documents

PHOTOCHEMICAL SYNTHESIS OF APORPHINES: (+/-)-THALIPORPHINE, (+/-)-N-METHYLLAUROTETANINE AND (+/-)-ISOBOLDINE.

Aporphines, (+/-)-thaliporphine (1), (+/-)-N-methyllaurotetaline (2), and (+/-)-isoboldine (3) were synthesised using photochemical cyclization as the key step.