10264-27-4

Basic information

• Product Name: N-cyclohexylhexanamide
• CAS NO: 10264-27-4
• Molecular Formula: C₁₂H₂₃NO
• Molecular Weight: 197.3171
• Mol File: 10264-27-4.mol
• Article Data: 5

Chemical Properties

• Boiling Point: 346.7°C at 760 mmHg
• Flash Point: 208.3°C
• Density: 0.92g/cm³
• Vapor Pressure: 5.65E-05mmHg at 25°C
• Refractive Index: 1.467
• CAS DataBase Reference: N-cyclohexylhexanamide(CAS DataBase Reference)
• NIST Chemistry Reference: N-cyclohexylhexanamide(10264-27-4)
• EPA Substance Registry System: N-cyclohexylhexanamide(10264-27-4)

Safety Data

• Hazardous Substances Data: 10264-27-4(Hazardous Substances Data)

Upstream product

• 2763-78-2 2-cyclohexyl-1-oxa-2-azaspiro[2.5]octane 
• 108-91-8 cyclohexylamine 
• 142-61-0 Hexanoyl chloride 
• 142-62-1 hexanoic acid 
• 2051-49-2 n-hexanoic anhydride 
• 106-70-7 methyl hexanoate 
• 123-66-0 Ethyl hexanoate 
• 3173-53-3 Cyclohexyl isocyanate 
• 2443-62-1 hexanoic acid hydrazide 

Downstream Products

• 4746-28-5 N-hexylcyclohexanamine 
• 30930-83-7 hexanal N-cyclohexylimine 
• 30930-83-7 hexanal cyclohexylimine 

Relevant articles and documents

N-Acyl-N-(4-chlorophenyl)-4-nitrobenzenesulfonamides: Highly selective and efficient reagents for acylation of amines in water

A variety of N-acyl-N-(4-chlorophenyl)-4-nitrobenzenesulfonamides (1a-e) were synthesized in one pot from 4-chloroaniline under solvent-free conditions and have been developed as chemoselective N-acylation reagents. Selective protection of primary amines in the presence of secondary amines, acylation of aliphatic amines in the presence of aryl amines, and monofunctionalization of primary-secondary diamines as well as selective N-acylation of amino alcohols using these reagents are described. All of the acylation reactions were carried out in water as a green solvent. High stability and easy preparation of these acylating reagents are other advantages of this method.

Tighter ion pair effect and scale-up study in microwave assisted aminolysis of enolizable esters using potassium tert-butoxide (t-BuOK)

The tighter ion pair effect and scale-up study in aminolysis of enolizable esters using potassium tert-butoxide (t-BuOK) under microwave irradiations is described. This method provides synthetic advantages in terms of reaction time, product yields, eco-friendly environment and scale-up feasibility over the conventional heating method.

A novel dehydrazination reaction. V. The formation of various amides from aliphatic and aromatic carboxylic acid hydrazides in the presence of chloral.

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