83367-37-7

Basic information

• Product Name: 2H,4H-Oxazolo[5,4,3-ij]quinoline-4-thione, 6,7-dimethyl-
• Synonyms: 2H,4H-Oxazolo[5,4,3-ij]quinoline-4-thione, 6,7-dimethyl-
• CAS NO: 83367-37-7
• Molecular Formula: C12H11NOS
• Molecular Weight: 0
• Mol File: 83367-37-7.mol
• Article Data: 0

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2H,4H-Oxazolo[5,4,3-ij]quinoline-4-thione, 6,7-dimethyl-(CAS DataBase Reference)
• NIST Chemistry Reference: 2H,4H-Oxazolo[5,4,3-ij]quinoline-4-thione, 6,7-dimethyl-(83367-37-7)
• EPA Substance Registry System: 2H,4H-Oxazolo[5,4,3-ij]quinoline-4-thione, 6,7-dimethyl-(83367-37-7)

Safety Data

• Hazardous Substances Data: 83367-37-7(Hazardous Substances Data)

Usage

Description

2H,4H-Oxazolo[5,4,3-ij]quinoline-4-thione, 6,7-dimethylis a complex chemical compound characterized by an oxazoloquinoline ring system and a thione functional group. This yellow solid compound is utilized in the synthesis of pharmaceuticals and agrochemicals, and has been investigated for its antimicrobial and anti-inflammatory properties. Its structure, which includes a thione group, also indicates potential use as a sulfur-containing reagent in organic synthesis.

Uses

Used in Pharmaceutical and Agrochemical Industries:
2H,4H-Oxazolo[5,4,3-ij]quinoline-4-thione, 6,7-dimethylis used as an intermediate in the preparation of various pharmaceuticals and agrochemicals due to its unique molecular structure and potential medicinal properties.
Used in Organic Synthesis:
2H,4H-Oxazolo[5,4,3-ij]quinoline-4-thione, 6,7-dimethylis used as a sulfur-containing reagent in organic synthesis, taking advantage of the reactivity and functional group presence in its structure.
Used in Medicinal Research:
2H,4H-Oxazolo[5,4,3-ij]quinoline-4-thione, 6,7-dimethylis used in medicinal research for its potential antimicrobial and anti-inflammatory effects, making it a candidate for the development of new therapeutic agents.
Used in Heterocyclic Compound Synthesis:
As a building block, this compound is utilized in the synthesis of various heterocyclic compounds, contributing to the diversity and complexity of organic chemistry.