146710-02-3

Basic information

• Product Name: 2-(methoxycarbonyl)-9-methyl-1H-pyrrolo[3,2-h]quinolin-9-ium iodide
• CAS NO: 146710-02-3
• Molecular Formula: C₁₄H₁₃IN₂O₂
• Molecular Weight: 368.1697
• Mol File: 146710-02-3.mol
• Article Data: 0

Chemical Properties

• CAS DataBase Reference: 2-(methoxycarbonyl)-9-methyl-1H-pyrrolo[3,2-h]quinolin-9-ium iodide(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(methoxycarbonyl)-9-methyl-1H-pyrrolo[3,2-h]quinolin-9-ium iodide(146710-02-3)
• EPA Substance Registry System: 2-(methoxycarbonyl)-9-methyl-1H-pyrrolo[3,2-h]quinolin-9-ium iodide(146710-02-3)

Safety Data

• Hazardous Substances Data: 146710-02-3(Hazardous Substances Data)

Usage

Pyrroloquinoline derivative

The compound is derived from a pyrroloquinoline structure, which is a fused ring system consisting of a pyrrole ring and a quinoline ring.

Quinoline ring system

The compound contains a quinoline ring system, which is a tricyclic aromatic compound with a chemical structure consisting of a benzene ring fused to a pyridine ring.

Pyrrole ring

The compound has a pyrrole ring fused to the quinoline ring system, which is a five-membered ring with alternating single and double bonds and a nitrogen atom at one end.

Methoxycarbonyl group

The compound contains a methoxycarbonyl group (-COOCH3), which is a carbonyl group attached to a methoxy group (-OCH3).

Methyl group

The compound also contains a methyl group (-CH3), which is a carbon atom attached to three hydrogen atoms.

Iodide ion

The compound contains an iodide ion (I-), which is a negatively charged ion formed when iodine gains an electron.

Salt

The presence of the iodide ion makes this compound a salt, which is a compound formed by the neutralization of an acid and a base.

Organic synthesis and medicinal chemistry

The compound is commonly used in organic synthesis and medicinal chemistry, which are fields of chemistry focused on the synthesis and study of organic compounds.

Nucleophilic substitutions

The compound is used in various organic reactions, including nucleophilic substitutions, which are reactions in which a nucleophile (an electron-rich species) replaces a leaving group in a molecule.

Cyclizations

The compound is also used in cyclizations, which are reactions in which a ring structure is formed in a molecule.

Reagent for the synthesis of other organic compounds

The compound is used as a reagent in the synthesis of other organic compounds, which are molecules containing carbon.

Development of pharmaceuticals and bioactive molecules

The properties and reactivity of the compound make it a valuable tool for the development of pharmaceuticals and bioactive molecules, which are compounds that have a biological effect on living organisms.