1194-66-7

Basic information

• Product Name: 2,6-DICHLORONITROSOBENZENE
• Synonyms: 2,6-DICHLORONITROSOBENZENE;1,3-Dichloro-2-nitrosobenzene;2,6-DICHLORONITROSOBENZENE 98%
• CAS NO: 1194-66-7
• Molecular Formula: C₆H₃Cl₂NO
• Molecular Weight: 176
• Mol File: 1194-66-7.mol

Chemical Properties

• Melting Point: 170-171°C
• Boiling Point: 271.9 °C at 760 mmHg
• Flash Point: 120.5 °C
• Appearance: /
• Density: 1.45 g/cm³
• Vapor Pressure: 0.0105mmHg at 25°C
• Refractive Index: 1.588
• CAS DataBase Reference: 2,6-DICHLORONITROSOBENZENE(CAS DataBase Reference)
• NIST Chemistry Reference: 2,6-DICHLORONITROSOBENZENE(1194-66-7)
• EPA Substance Registry System: 2,6-DICHLORONITROSOBENZENE(1194-66-7)

Safety Data

• Statements: 36/37/38
• Safety Statements: 26-36
• Hazardous Substances Data: 1194-66-7(Hazardous Substances Data)

Usage

Uses

Used in Chemical Synthesis:
2,6-Dichloronitrosobenzene is used as a key intermediate in the synthesis of various complex organic compounds. Its unique structure allows for the creation of a wide range of molecules, making it a valuable asset in the field of chemical synthesis.
Used in Research Applications:
In the research industry, 2,6-Dichloronitrosobenzene is employed as a reagent for studying chemical reactions and mechanisms. Its properties and reactivity provide insights into the behavior of nitroso compounds and dichlorobenzene derivatives, contributing to the advancement of scientific knowledge.
Used in Industrial Settings:
2,6-Dichloronitrosobenzene is used as a building block in the production of various industrial chemicals. Its versatility in synthesis allows for the creation of a diverse range of products, making it an important component in the manufacturing process.
Used in Environmental Mitigation:
Despite its potential environmental harm, 2,6-Dichloronitrosobenzene can be used in the development of methods to mitigate the risks associated with its toxicity. By understanding its properties and reactivity, researchers can develop safer handling procedures and waste disposal techniques, reducing the environmental impact of this chemical.

InChI:InChI=1/C6H3Cl2NO/c7-4-2-1-3-5(8)6(4)9-10/h1-3H

Upstream product

• 6579-27-7 2,6-Dichloro-N-hydroxybenzenecarboximidoyl chloride 
• 3032-92-6 4-cyanophenylacetylene 
• 100045-99-6 2,6-dichloronitrosobenzene dimer 
• 608-31-1 2,6-Dichloroaniline 

Downstream Products

• 863975-19-3 3-(2,6-dichlorophenyl)-5-(4-cyanophenyl)isoxazole 
• 81432-12-4 (S)-1-(7-Nitro-benzo[1,2,5]oxadiazol-4-yl)-pyrrolidine-2-carboxylic acid 
• 174844-42-9 2-(N-(7-nitrobenz-2-oxa-1,3-diazol-4-yl)amino)-2-deoxyglucose 
• 927664-20-8 C₁₅H₁₄N₄O₄ 
• 1060798-84-6 4-(dimethylamino)-2,6-dichloronitrosobenzene 
• 916853-01-5 μ2-(η2-N,O-2,6-dichloronitrosobenzene)bis[μ-bromotricarbonylrhenium(I)] 
• 18378-29-5 4-methylamino-7-nitro-2,1,3-benzoxadiazole 
• 1455-87-4 N,N-dimethyl-7-nitrobenzo[c][1,2,5]oxadiazol-4-amine 
• 10199-91-4 4-amino-7-nitro-2,1,3-benzoxadiazole 
• 10199-89-0 NBD chloride 
• 18378-20-6 N-benzyl-7-nitrobenzo[c][1,2,5]oxadiazol-4-amine 
• 10199-87-8 2,4-dinitro-1,3-phenylenediamine 
• 100045-99-6 2,6-dichloronitrosobenzene dimer 
• 601-88-7 2,6-dichloronitrobenzene 

Relevant articles and documents

Improved synthesis of 4-amino-7-nitrobenz-2,1,3-oxadiazoles using NBD fluoride (NBD-F)

The 7-nitrobenz-2,1,3-oxadiazole (NBD) unit is a highly useful fluorescent tag with wide application in biology. Installation of the NBD group typically proceeds via the SNAr reaction between an amine and an NBD halide. Herein, we demonstrate that NBD-F 1 results in significantly higher yields than NBD-Cl 2, and that triethylamine in dimethylformamide at 23 °C overnight is a broadly applicable set of conditions for this reaction. In particular, the highly useful fluorescent carbohydrate 2-NBD-glucosamine (2-NBDG, 3) can now be prepared in 75% yield with NBD-F as compared to 12% with NBD-Cl.

HETEROCYCLIC COMPOUNDS HAVING AN OXADIAZOLE MOIETY AND HYDRO ISOMERS THEREOF

The present invention relates to substituted diphenyl heterocycle compounds having an oxadiazole moiety and pharmaceuticals compositions thereof that inhibit replication of HCV virus. The present invention also relates to the use of the compounds and/or compositions to inhibit HCV replication and/or proliferation and to treat or prevent HCV infections.

PRESSURE EFFECT ON DIMERIZATION EQUILIBRIA OF A SERIES OF SUBSTITUTED NITROSOBENZENES IN SOLUTION.

The effect of pressure was studied on the dimerization reactions of six di- and tri-substituted nitrosobenzenes in carbon tetrachloride at 25 degree C. The obtained configurational volume changes for the prototype one bond formation reactions are in the range of minus 17 to minus 21 cm**3 mol** minus **1 at 6. 13 MPa. The volume changes were interpreted in terms of the perturbation theory of liquid; they were dominated by the volume change in the reference system composed of hard spheres. Small differences between the observed and theoretical reference volume changes were ascribed to the perturbation due to electrostatic interactions between the solute and solvent; the perturbation volume changes were estimated by the Kirkwood theory of dipolar solvation.

OXIDATION OF HYDRAZINES WITH NITROSOBENZENES

Nitrosoarenes react with 1,1-disubstituted hydrazines to yield products of direct oxidation and the thermally stable triazene N-oxides.The triazene N-oxides undergo photoinduced fragmentation to yield products which may be rationalized through the interme