68834-07-1

Basic information

• Product Name: 2-[[[[4,6-bis[bis(methoxymethyl)amino]-1,3,5-triazin-2-yl](methoxymethyl)amino]methyl]amino]-9-methoxy-1H-xantheno[2,1,9-def]isoquinoline-1,3(2H)-dione
• Synonyms: 1H-Xantheno(2,1,9-def)isoquinoline-1,3(2H)-dione, 2-((((4,6-bis(bis(methoxymethyl)amino)-1,3,5-triazin-2-yl)(methoxymethyl)amino)methyl)amino)-9-methoxy-; 2-((((4,6-Bis(bis(methoxymethyl)amino)-1,3,5-triazin-2-yl)(methoxymethyl)amino)methyl)amino)-9-methoxy-1H-xantheno(2,1,9-def)isoquinoline-1,3(2H)-dione; 2-({[{4,6-bis[bis(methoxymethyl)amino]-1,3,5-triazin-2-yl}(methoxymethyl)amino]methyl}amino)-9-methoxy-1H-benzo[3,4]isochromeno[7,8,1-def]isoquinoline-1,3(2H)-dione
• CAS NO: 68834-07-1
• Molecular Formula: C₃₃H₃₈N₈O₉
• Molecular Weight: 690.703
• EINECS: 272-433-5
• Mol File: 68834-07-1.mol
• Article Data: 0

Chemical Properties

• Boiling Point: 851.1°C at 760 mmHg
• Flash Point: 468.5°C
• Density: 1.45g/cm³
• Vapor Pressure: 2.9E-29mmHg at 25°C
• Refractive Index: 1.68
• CAS DataBase Reference: 2-[[[[4,6-bis[bis(methoxymethyl)amino]-1,3,5-triazin-2-yl](methoxymethyl)amino]methyl]amino]-9-methoxy-1H-xantheno[2,1,9-def]isoquinoline-1,3(2H)-dione(CAS DataBase Reference)
• NIST Chemistry Reference: 2-[[[[4,6-bis[bis(methoxymethyl)amino]-1,3,5-triazin-2-yl](methoxymethyl)amino]methyl]amino]-9-methoxy-1H-xantheno[2,1,9-def]isoquinoline-1,3(2H)-dione(68834-07-1)
• EPA Substance Registry System: 2-[[[[4,6-bis[bis(methoxymethyl)amino]-1,3,5-triazin-2-yl](methoxymethyl)amino]methyl]amino]-9-methoxy-1H-xantheno[2,1,9-def]isoquinoline-1,3(2H)-dione(68834-07-1)

Safety Data

• Hazardous Substances Data: 68834-07-1(Hazardous Substances Data)

Usage

Molecular structure

The compound has a long and intricate molecular structure with multiple triazine, xantheno, and isoquinoline functional groups, as well as methoxymethyl and amino substituents.

Triazine group

The presence of a 1,3,5-triazine core structure in the molecule contributes to its potential chemical and biological properties.

Xantheno and isoquinoline groups

These heterocyclic structures are known for their ability to interact with biological targets, such as enzymes, receptors, or nucleic acids.

Methoxymethyl substituents

These groups are attached to the carbon atoms in the xantheno and isoquinoline rings, which may influence the compound's solubility, stability, and reactivity.

Amino substituents

The presence of amino groups in the molecule can contribute to hydrogen bonding and other interactions with biological targets.

Potential diverse chemical and biological properties

Due to its complex structure and various functional groups, the compound may exhibit a range of chemical and biological activities.

Interaction with biological targets

The compound has the potential to interact with various biological targets, such as enzymes, receptors, or nucleic acids, which could lead to potential applications in drug development or other fields.

Need for further research

To fully understand and characterize the chemical and biological behavior of this compound, additional research and investigations are required.