39060-31-6

Basic information

• Product Name: 5-CHLORBENZOFURAZAN-3-OXIDE
• Synonyms: 5-CHLORBENZOFURAZAN-3-OXIDE;5-CHLOROBENZOFURAZAN 3-OXIDE;LABOTEST-BB LT00138239;5-CHLORBENZOFURAN-3-OXIDE;5-chlorobenzofuran 3-oxide;5-chloro-3-oxido-2,1,3-benzoxadiazol-3-ium
• CAS NO: 39060-31-6
• Molecular Formula: C₆H₃ClN₂O₂
• Molecular Weight: 170.55
• Product Categories: OxadiazolesHeterocyclic Building Blocks;Building Blocks;Halogenated Heterocycles;Heterocyclic Building Blocks;Oxadiazoles
• Mol File: 39060-31-6.mol
• Article Data: 2

Chemical Properties

• Melting Point: 47-48 °C(lit.)
• Boiling Point: 287.1°Cat760mmHg
• Flash Point: 127.4°C
• Appearance: /
• Density: 1.69g/cm³
• Vapor Pressure: 0.00438mmHg at 25°C
• Refractive Index: 1.701
• CAS DataBase Reference: 5-CHLORBENZOFURAZAN-3-OXIDE(CAS DataBase Reference)
• NIST Chemistry Reference: 5-CHLORBENZOFURAZAN-3-OXIDE(39060-31-6)
• EPA Substance Registry System: 5-CHLORBENZOFURAZAN-3-OXIDE(39060-31-6)

Safety Data

• Hazard Codes: Xi
• Statements: 36/37/38
• Safety Statements: 26-36
• WGK Germany: 3
• Hazardous Substances Data: 39060-31-6(Hazardous Substances Data)

Usage

General Description

5-CHLORBENZOFURAZAN-3-OXIDE is a chemical compound with the molecular formula C7H3ClN2O2. It is a heterocyclic compound consisting of a benzofurazan ring with a chlorine atom attached to the 5-position. 5-CHLORBENZOFURAZAN-3-OXIDE is known for its strong oxidizing properties and is often used as a reagent in organic synthesis reactions. It is also utilized as a dye for fluorescent labeling and detection of protein and amino acid derivatives. Additionally, 5-CHLORBENZOFURAZAN-3-OXIDE has been studied for potential applications in the development of new materials and pharmaceutical compounds. Due to its reactive nature, it is important to handle this compound with caution and follow proper safety guidelines when working with it in a laboratory setting.

InChI:InChI=1/C6H3ClN2O2/c7-4-1-2-5-6(3-4)9(10)11-8-5/h1-3H

Upstream product

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• 1253058-88-6 7-chloro-3-phenylquinoxaline-2-carboxylic acid (2-phenylethyl)amide 1,4-di-N-oxide 

Relevant articles and documents

1,2,3-Triazolo [1,5-a][1,4]- and 1,2,3-triazolo[l,5-a]-[1,5]benzodiazepine derivatives: Synthesis and benzodiazepine receptor binding

This paper reports the synthesis of new 1,2,3-triazolo[1,4]benzodiazepine and 1,2,3-triazolo[1,5]benzodiazepine derivatives and their evaluation toward benzodiazepine receptors. Receptor affinity gradually and remarkably increases by moving the nitrogen atom of the central ring from position 3 through 4 to position 5, to give the most effective compound 6a (K(i) = 150 nM). N-methylation of the diazepine ring (7a) lowers receptorial binding. Introduction of a chlorine atom on the benzene ring doubles the K(i) value (6b) which remains unaltered by the N-methylation (7b).