2427-71-6

Basic information

• Product Name: 2-Hydroxy-6-chloroquinoxaline
• Synonyms: 6-chloro-2(1h)-quinoxalinon;2-HYDROXY-6-CHLOROQUINOXALINE;6-CHLORO-2(1H)-QUINOXALINONE;6-CHLORO-2-HYDROXYQUINOXALINE;6-chloroquinoxalin-2(1H)-one;6-Chloroquinoxalin-2-ol;2(1H)-Quinoxalinone,6-chloro-;6-Chloroquinoxaline-2(1H)-one
• CAS NO: 2427-71-6
• Molecular Formula: C₈H₅ClN₂O
• Molecular Weight: 180.59
• Product Categories: Miscellaneous
• Mol File: 2427-71-6.mol
• Article Data: 3

Chemical Properties

• Melting Point: 305 °C
• Boiling Point: 396.5 °C at 760 mmHg
• Flash Point: 193.6 °C
• Appearance: Crystalline Powder
• Density: 1.5 g/cm³
• Vapor Pressure: 7.46E-07mmHg at 25°C
• Refractive Index: 1.688
• Storage Temp.: Sealed in dry,Room Temperature
• PKA: 8.10±0.70(Predicted)
• CAS DataBase Reference: 2-Hydroxy-6-chloroquinoxaline(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Hydroxy-6-chloroquinoxaline(2427-71-6)
• EPA Substance Registry System: 2-Hydroxy-6-chloroquinoxaline(2427-71-6)

Safety Data

• Hazardous Substances Data: 2427-71-6(Hazardous Substances Data)

Usage

Description

2-Hydroxy-6-chloroquinoxaline is a chemical compound with the molecular formula C7H4ClN2O2. It is a crystalline powder that serves as an intermediate in the production of herbicides. 2-Hydroxy-6-chloroquinoxaline is characterized by its hydroxyl and chloro substituents, which contribute to its reactivity and potential applications in various industries.

Uses

Used in Agricultural Industry:
2-Hydroxy-6-chloroquinoxaline is used as an intermediate for the production of herbicides. Its chemical properties, including the presence of a hydroxyl group and a chloro substituent, make it a valuable component in the synthesis of various herbicidal compounds. These herbicides are essential for controlling unwanted plant growth in agricultural settings, ensuring the healthy growth of crops and increasing overall yield.
Please note that the provided materials do not mention any other specific applications or industries for 2-Hydroxy-6-chloroquinoxaline. If there are additional uses or industries that utilize this compound, further information would be required to accurately describe them.

InChI:InChI=1/C8H5ClN2O/c9-5-1-2-6-7(3-5)10-4-8(12)11-6/h1-4H,(H,11,12)

Upstream product

• 34836-97-0 6-chloro-1,2-dihydro-2-oxoquinoxaline 4-oxide 
• 924-44-7 glyoxylic acid ethyl ester 
• 95-83-0 4-Chloro-1,2-phenylenediamine 

Downstream Products

• 18671-97-1 2,6-dichloroquinoxaline 
• 1448-87-9 2-chloroquinoxaline 
• 89938-22-7 6-chloro-1,2,3,4-tetrahydroquinoxalin-2-one 
• 1315337-00-8 6-chloro-2-(perfluorophenyl)quinoxaline 
• 1240616-87-8 2-bromo-6-chloroquinoxaline 
• 33488-35-6 6-Chloro-3-phenylquinoxalin-2(1H)-one 

Relevant articles and documents

Electro-oxidative C-H alkylation of quinoxalin-2(1: H)-ones with organoboron compounds

Radical cleavage of C-B bonds to accomplish C-H functionalization is synthetically appealing but practically challenging. We report herein a mild electro-oxidative method for efficient C-H alkylation of quinoxalin-2(1H)-ones by means of radical addition reactions of alkyl boronic acids and esters and alkyl trifluoroborates to afford C-C coupled products. This journal is

The facile one pot synthesis of 6-substituted 2(1H)-quinoxalinones

Facile one pot synthesis of 6-substituted 2(1H)-quinoxalinones and these reaction mechanisms are described.The intramolecular cyclization reaction of 4'-substituted 2'-nitroacetoacetanilides in aqueous basic medium and the reduction of 6-substituted 2(1H)-quinoxalinone-4-oxide wit sodium borohydride or sodium hydrogensulfite were studied in detail