13665-49-1

Basic information

• Product Name: pentachloronitrosobenzene
• Synonyms: pentachloronitrosobenzene
• CAS NO: 13665-49-1
• Molecular Formula: C₆Cl₅NO
• Molecular Weight: 279.34
• Mol File: 13665-49-1.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 385.7°C at 760 mmHg
• Flash Point: 171.2°C
• Appearance: /
• Density: 1.87g/cm³
• Vapor Pressure: 8.32E-06mmHg at 25°C
• Refractive Index: 1.652
• CAS DataBase Reference: pentachloronitrosobenzene(CAS DataBase Reference)
• NIST Chemistry Reference: pentachloronitrosobenzene(13665-49-1)
• EPA Substance Registry System: pentachloronitrosobenzene(13665-49-1)

Safety Data

• Hazardous Substances Data: 13665-49-1(Hazardous Substances Data)

Usage

InChI:InChI=1/C6Cl5NO/c7-1-2(8)4(10)6(12-13)5(11)3(1)9

Upstream product

• 118-74-1 hexachlorobenzene 
• 527-20-8 2,3,4,5,6-pentachloroaniline 

Downstream Products

• 35191-76-5 2,3,4,5,6-Pentachloro-4'-brom-azobenzol 
• 22876-48-8 Pentachlorphenyl-hydroxylamin 
• 69576-80-3 1,2,3,4-Tetrachlor-5-methoxy-6-nitrobenzol 
• 22876-54-6 1.2.3.4-Tetrachlor-5-cyclohexyl-amino-6-nitro-benzol 
• 22876-55-7 1.2.4.5-Tetrachlor-3-cyclohexyl-amino-6-nitro-benzol 
• 2438-88-2 2,3,5,6-tetrachloro-4-nitro-anisole 
• 20098-38-8 1,2,4,5-tetrachloro-3,6-dinitrobenzene 
• 35159-18-3 4'-Methoxy-2,3,4,5,6-pentachloroazoxybenzol 
• 35159-12-7 2,3,4,5,6-Pentachloro-4'-bromo-azoxybenzol 
• 35159-16-1 2,3,4,4',5,6-Hexachlor-azoxybenzol 
• 781-15-7 1,2,3,4-tetrachloro-5,6-dinitrobenzene 
• 35159-15-0 2,3,4,4',5,6-Hexachlor-azobenzol 
• 35159-13-8 4'-Methyl-2,3,4,5,6-pentachloroazobenzol 
• 82-68-8 Quintozene 

Related news

Basic metabolites of pentachloronitrosobenzene (cas 13665-49-1) (PCNO) in livers of female rats09/06/2019

Pentachloroaniline, 2,3,5,6-tetrachloroaniline, 2,3,4,6-tetrachloroaniline, and 2,3,4,5-tetrachloroaniline were identified as metabolites of pentachloronitrosobenzene in livers of female rats.detailed

Relevant articles and documents

Epoxy-epimination of cyclic conjugated dienes - VII. Cycloaddition of nitroso-halogenobenzenes to cyclopentadiene followed by rearrangement to epoxy-epimino- and γ-δ-epiminopentadienal derivatives via N-O and C-C bond breaking

[4 + 2] Cycloaddition of halogenated nitroso benzenes to cyclopentadiene followed by isomerisation of the intermediated adduct occurs already at room temperature to furnish the epoxy-epimine 1 and the epiminopentadienal 2. The structure proof of 1 is based on X-ray analysis.