695-64-7

Basic information

• Product Name: Cyclohexane, 1-chloro-1-nitroso-
• Synonyms: Cyclohexane, 1-chloro-1-nitroso-;α-chloronitrosocyclohexane;1-CHLORONITROSOCYCLOHEXANE
• CAS NO: 695-64-7
• Molecular Formula: C₆H₁₀ClNO
• Molecular Weight: 147.6027
• Mol File: 695-64-7.mol
• Article Data: 4

Chemical Properties

• Melting Point: 116.5°C
• Boiling Point: 62-63 °C(Press: 22 Torr)
• Appearance: /
• Density: 1.1140
• Refractive Index: 1.4870 (estimate)
• CAS DataBase Reference: Cyclohexane, 1-chloro-1-nitroso-(CAS DataBase Reference)
• NIST Chemistry Reference: Cyclohexane, 1-chloro-1-nitroso-(695-64-7)
• EPA Substance Registry System: Cyclohexane, 1-chloro-1-nitroso-(695-64-7)

Safety Data

• Hazard Codes: 3:
• Safety Statements: − and NOx." target="_blank">May explode during vacuum distillation. When heated to decomposition it emits toxic fumes of C
• Hazardous Substances Data: 695-64-7(Hazardous Substances Data)

Upstream product

• 7647-01-0 hydrogenchloride 
• 100-64-1 cyclohexanone-oxime 
• 7782-50-5 chlorine 
• 7732-18-5 water 
• 60-29-7 diethyl ether 
• 75157-19-6 tert-butyldimethylsilyl cyclohexylideneazinate 
• 1122-60-7 1-nitrocyclohexane 
• 2899-02-7 N,N'-dichlorobis(2,4,6-trichlorodiphenyl)urea 
• 110-82-7 cyclohexane 

Downstream Products

• 100-64-1 cyclohexanone-oxime 
• 873-92-7 1-chloro-1-nitrocyclohexane 
• 7160-44-3 2-oxa-3-azabicyclo[2.2.2]oct-5-ene 
• 371-90-4 1,1-difluorocyclohexane 
• 371-89-1 chlorofluorocyclohexane 
• 108-94-1 cyclohexanone 
• 7647-01-0 hydrogenchloride 
• 7782-77-6 cis-nitrous acid 
• 529-17-9 tropane 
• 95798-94-0 1-(<(benzyloxy)carbonyl>amino)-4-cycloheptene 
• 95798-93-9 1-(<(benzyloxy)carbonyl>amino)-3-cycloheptene 
• 95799-01-2 N-<(benzoyloxy)carbonyl>nortropane 
• 95798-95-1 trans-1-(<(benzyloxy)carbonyl>amino)4-chlorocycloheptane 
• 95798-92-8 cis-4-(<(benzyloxy)carbonyl>amino)cycloheptanol 

Relevant articles and documents

New and improved methods for the conversion of nitroalkanes into geminal chloronitroso compounds

The scope and limitations of a new method for the preparation of geminal chloronitroso compounds involving treatment of a nitronate anion with oxalyl chloride are described in full, and a milder, high yielding, and more chemoselective variant using the de

Generation of nitryl chloride from chlorotrimethylsilane-acetyl nitrate reaction: A one-pot preparation of gem-chloronitro compounds from oximes

While iso-amyl nitrite reacts with chlorotrimethylsilane to give NOCl, iso-amyl nitrate does not yield NO 2Cl with silicon reagent. However, acetyl nitrate reacts successfully with chlorotrimethylsilane to give nitryl chloride, which is charact