84218-45-1

Basic information

• Product Name: 2(1H)-Isoquinolinemethanamine, 3,4-dihydro-6,7-dimethoxy-N-(2-(3,4-dim ethoxyphenyl)ethyl)-1-(1H-indol-3-ylmethyl)-
• Synonyms: 2(1H)-Isoquinolinemethanamine, 3,4-dihydro-6,7-dimethoxy-N-(2-(3,4-dim ethoxyphenyl)ethyl)-1-(1H-indol-3-ylmethyl)-
• CAS NO: 84218-45-1
• Molecular Formula: C31H37 N3 O4
• Molecular Weight: 0
• Mol File: 84218-45-1.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 675.4°C at 760 mmHg
• Flash Point: 362.3°C
• Appearance: /
• Density: 1.178g/cm³
• Vapor Pressure: 4.23E-18mmHg at 25°C
• Refractive Index: 1.612
• CAS DataBase Reference: 2(1H)-Isoquinolinemethanamine, 3,4-dihydro-6,7-dimethoxy-N-(2-(3,4-dim ethoxyphenyl)ethyl)-1-(1H-indol-3-ylmethyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: 2(1H)-Isoquinolinemethanamine, 3,4-dihydro-6,7-dimethoxy-N-(2-(3,4-dim ethoxyphenyl)ethyl)-1-(1H-indol-3-ylmethyl)-(84218-45-1)
• EPA Substance Registry System: 2(1H)-Isoquinolinemethanamine, 3,4-dihydro-6,7-dimethoxy-N-(2-(3,4-dim ethoxyphenyl)ethyl)-1-(1H-indol-3-ylmethyl)-(84218-45-1)

Safety Data

• Hazardous Substances Data: 84218-45-1(Hazardous Substances Data)

Usage

3,4-Dihydro

The presence of two hydrogen atoms attached to the isoquinoline ring, indicating a reduced form of the compound and potentially affecting its reactivity and properties.

6,7-Dimethoxy

Two methoxy groups (-OCH3) attached to the isoquinoline ring at the 6 and 7 positions, which can influence the compound's solubility, stability, and interaction with other molecules.

1-(1H-indol-3-ylmethyl)

A 1H-indol-3-ylmethyl group (a derivative of the indole ring system) attached to the nitrogen atom. This group can influence the compound's solubility, stability, and interaction with other molecules, as well as contribute to its potential biological activity.

Amine functional group

A nitrogen atom bonded to a hydrogen atom and an alkyl group (in this case, the 1-(1H-indol-3-ylmethyl) group). The amine group can participate in hydrogen bonding and other interactions, which can affect the compound's solubility, stability, and biological activity.

Specific uses and properties

The specific uses and properties of this compound would depend on the context of its intended application, such as its potential role in drug development, therapeutic interventions, or chemical research.

InChI:InChI=1/C31H37N3O4/c1-35-28-10-9-21(15-29(28)36-2)11-13-32-20-34-14-12-22-17-30(37-3)31(38-4)18-25(22)27(34)16-23-19-33-26-8-6-5-7-24(23)26/h5-10,15,17-19,27,32-33H,11-14,16,20H2,1-4H3

Upstream product

• 50-00-0 formaldehyd 
• 120-20-7 2-(3,4-dimethoxyphenyl)-ethylamine 
• 15832-21-0 1-((1H-indol-3-yl)methyl)-6,7-dimethoxy-1,2,3,4-tetrahydroisoquinoline 

Relevant articles and documents

Antiinflammatory and antiproteolytic activities of newer indolyl isoquinolines

Several indolyl isoquinoline derivatives were synthesized and evaluated for their antiinflammatory and antiproteolytic activities. These derivatives possessed 9.2-32.4% inhibition at a dose of 100 mg/kg i.p. against carrageenin-induced oedema. Four of the