116855-58-4

Basic information

• Product Name: (cyclohexylmethyl)(prop-2-en-1-yl)amine
• Synonyms: (cyclohexylmethyl)(prop-2-en-1-yl)amine
• CAS NO: 116855-58-4
• Molecular Formula: C₁₀H₁₉N
• Molecular Weight: 153.26
• Mol File: 116855-58-4.mol
• Article Data: 6

Chemical Properties

• Boiling Point: 216.6±9.0 °C(Predicted)
• Appearance: /
• Density: 0.846±0.06 g/cm3(Predicted)
• PKA: 10.13±0.20(Predicted)
• CAS DataBase Reference: (cyclohexylmethyl)(prop-2-en-1-yl)amine(CAS DataBase Reference)
• NIST Chemistry Reference: (cyclohexylmethyl)(prop-2-en-1-yl)amine(116855-58-4)
• EPA Substance Registry System: (cyclohexylmethyl)(prop-2-en-1-yl)amine(116855-58-4)

Safety Data

• Hazardous Substances Data: 116855-58-4(Hazardous Substances Data)

Usage

General Description

The chemical (cyclohexylmethyl)(prop-2-en-1-yl)amine, also known as cyclohexylmethylallylamine, is an organic compound with the formula C10H17N. It is a tertiary amine that contains a cyclohexylmethyl group and a prop-2-en-1-yl group attached to the nitrogen atom. (cyclohexylmethyl)(prop-2-en-1-yl)amine is often used as a building block in the synthesis of various organic compounds, including pharmaceuticals, agrochemicals, and fine chemicals. Its specific chemical properties and potential applications may vary depending on the intended use and the specific chemical reactions and processes involved.

Upstream product

• 2043-61-0 cyclohexanecarbaldehyde 
• 107-11-9 1-amino-2-propene 
• 60-29-7 diethyl ether 
• 7732-18-5 water 

Downstream Products

• 1344667-71-5 2-allyl-6-methylbenzoic acid 
• 924276-82-4 methyl 3-(N-allyl-N-cyclohexylmethylamino)-2-methylpropionate 
• 924276-89-1 methyl 30(N-allyl-N-cyclohexylmethylamino)propionate 

Relevant articles and documents

Reductive Amination Revisited: Reduction of Aldimines with Trichlorosilane Catalyzed by Dimethylformamide─Functional Group Tolerance, Scope, and Limitations

Aldimines, generated in situ from aliphatic, aromatic, and heteroaromatic aldehydes and aliphatic, aromatic, and heteroaromatic primary or secondary amines, can be reduced with trichlorosilane in the presence of dimethylformamide (DMF) as an organocatalys

Nickel(II) Catalyzed Hydroboration: A Route to Selective Reduction of Aldehydes and N-Allylimines

A cationic [(iminophosphine)nickel(allyl)]+ complex was found to be sufficiently electrophilic to activate aldehydes and N-allylimines to undergo hydroboration with pinacolborane (HBpin) under mild reaction conditions. The catalyst displayed excellent selectivity toward aldehydes in the presence of ketones. A wide variety of functional groups were tolerated, including halogens, NO2, CN, OMe, and alkenes for both aldehydes and imines. Electron-rich substrates were found to be significantly more reactive than their electron poor counterparts, a feature that was correlated to their enhanced ability to coordinate to the Lewis acidic nickel center.

Diastereocontrolled synthesis of enantioenriched 3,4-disubstituted β-prolines

Enantioenriched 3,4-disubstituted β-prolines have been prepared with a high diastereocontrol through a carbometalation reaction or through a domino Michael addition/carbometalation reaction.