7175-49-7

Basic information

• Product Name: N-ETHYLDICYCLOHEXYLAMINE
• Synonyms: N-ETHYLDICYCLOHEXYLAMINE;N,N-DICYCLOHEXYLETHYLAMINE;Cyclohexanamine, N-cyclohexyl-N-ethyl-;Dicyclohexylamine, N-ethyl-;n-cyclohexyl-n-ethyl-cyclohexanamin;N-Cyclohexyl-N-ethylcyclohexanamine;n-ethyl-dicyclohexylamin;N-cyclohexyl-N-ethylcyclohexylamine
• CAS NO: 7175-49-7
• Molecular Formula: C₁₄H₂₇N
• Molecular Weight: 209.37
• EINECS: 230-534-1
• Product Categories: Amines;Building Blocks;C14 to C16;Chemical Synthesis;Nitrogen Compounds;Organic Building Blocks
• Mol File: 7175-49-7.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 114-115 °C3 mm Hg(lit.)
• Flash Point: >230 °F
• Appearance: Clear colorless/Liquid
• Density: 0.91 g/mL at 20 °C(lit.)
• Vapor Pressure: 0.00507mmHg at 25°C
• Refractive Index: n20/D 1.485(lit.)
• PKA: 11.11±0.20(Predicted)
• BRN: 2240256
• CAS DataBase Reference: N-ETHYLDICYCLOHEXYLAMINE(CAS DataBase Reference)
• NIST Chemistry Reference: N-ETHYLDICYCLOHEXYLAMINE(7175-49-7)
• EPA Substance Registry System: N-ETHYLDICYCLOHEXYLAMINE(7175-49-7)

Safety Data

• Hazard Codes: C
• Statements: 34
• Safety Statements: 26-36/37/39-45
• RIDADR: UN 2735 8/PG 2
• WGK Germany: 3
• RTECS: HY4150000
• HazardClass: 8
• PackingGroup: III
• Hazardous Substances Data: 7175-49-7(Hazardous Substances Data)

Usage

Chemical Properties

clear colorless liquid

Uses

N-Ethyldicyclohexylamine was used in the synthesis of F-amines along with other products by undergoing incomplete fluorination and fragmentation reactions.

InChI:InChI=1/C14H27N/c1-2-15(13-9-5-3-6-10-13)14-11-7-4-8-12-14/h13-14H,2-12H2,1H3/p+1

Upstream product

• 627-45-2 N-formylethylamine 
• 108-94-1 cyclohexanone 
• 103-69-5 N-ethyl-N-phenylamine 
• 75-03-6 ethyl iodide 
• 101-83-7 N-cyclohexyl-cyclohexanamine 
• 64-19-7 acetic acid 
• 64-67-5 diethyl sulfate 

Downstream Products

• 820969-07-1 [Ph2B(CH2PPh2)2]Pd(N,C:η2-NCy2CHCH3) 
• 100-19-6 (4-nitrophenyl)ethanone 
• 4727-98-4 1,1,3,3-tetrabenzoylpropane 
• 10536-76-2 p-bromophenacyl formate 
• 90273-33-9 2-Oxo-2-(4-chlorophenyl)ethyl formate 
• 111-34-2 -butyl vinyl ether 

Relevant articles and documents

Deoxygenation of tertiary amine N-oxides under metal free condition using phenylboronic acid

A simple and efficient method for the deoxygenation of amine N-oxides to corresponding amines is reported using the green and economical reagent phenylboronic acid. Deoxygenation of N,N-dialkylaniline N-oxides, trialkylamine N-oxides and pyridine N-oxides were achieved in good to excellent yields. The reduction susceptible functional groups such as ketone, amide, ester and nitro groups are well tolerated with phenylboronic acid during the deoxygenation process even at high temperature. In addition, an indirect method for identification and quantification of tert-amine N-oxide is demonstrated using UV–Vis spectrometry which may be useful for drug metabolism studies.