27375-04-8

Basic information

• Product Name: 1-amino-3,8-dichlorophenanthridin-6(5H)-one
• CAS NO: 27375-04-8
• Molecular Formula: C₁₃H₈Cl₂N₂O
• Molecular Weight: 279.1214
• Mol File: 27375-04-8.mol
• Article Data: 0

Chemical Properties

• Boiling Point: 412.7°C at 760 mmHg
• Flash Point: 203.4°C
• Density: 1.51g/cm³
• Vapor Pressure: 5.07E-07mmHg at 25°C
• Refractive Index: 1.698
• CAS DataBase Reference: 1-amino-3,8-dichlorophenanthridin-6(5H)-one(CAS DataBase Reference)
• NIST Chemistry Reference: 1-amino-3,8-dichlorophenanthridin-6(5H)-one(27375-04-8)
• EPA Substance Registry System: 1-amino-3,8-dichlorophenanthridin-6(5H)-one(27375-04-8)

Safety Data

• Hazardous Substances Data: 27375-04-8(Hazardous Substances Data)

Usage

Chemical structure

A phenanthridinone core with an amino group at position 1 and chloro substituents at positions 3 and 8.

Classification

Heterocyclic organic compound.

Potential applications

Pharmaceutical, dyes, and agrochemical industries.

Versatility

Presence of both amino and chloro groups makes it a valuable building block for the synthesis of more complex molecules.

Biological activity

Structural features suggest potential for biological activity, which could be valuable for drug discovery and development.

Importance

Understanding its properties and potential uses could lead to advancements in medicinal chemistry and other scientific disciplines.

Molecular weight

Approximately 271.12 g/mol (based on the molecular formula).

Functional groups

Amino (-NH2), chloro (-Cl), and carbonyl (C=O) groups.

Reactivity

May undergo reactions such as nucleophilic substitution, electrophilic aromatic substitution, and amide bond formation due to the presence of reactive functional groups.

Solubility

Likely to be soluble in organic solvents like dimethyl sulfoxide (DMSO), methanol, or acetonitrile, but solubility in water may be limited.

Stability

May be sensitive to light, heat, or moisture, and should be stored under appropriate conditions to maintain stability.

Analytical techniques

Techniques such as nuclear magnetic resonance (NMR), mass spectrometry (MS), and infrared (IR) spectroscopy can be used to analyze and confirm its structure.

Synthesis

Can be synthesized through various methods, such as the reaction of a phenanthridinone derivative with a suitable chlorinating agent and subsequent amination.

Safety precautions

Due to its complex structure and potential reactivity, appropriate safety measures should be taken when handling, such as wearing gloves, using a fume hood, and following proper disposal procedures.