41040-63-5

Basic information

• Product Name: 1-Pentyn-3-amine, N-butyl-3-methyl-
• Synonyms: Butyl-(1-ethyl-1-methyl-prop-2-ynyl)-amine;3-n-butylamino-3-methyl-1-pentyne
• CAS NO: 41040-63-5
• Molecular Formula: C10H19N
• Molecular Weight: 153.268
• Mol File: 41040-63-5.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 1-Pentyn-3-amine, N-butyl-3-methyl-(CAS DataBase Reference)
• NIST Chemistry Reference: 1-Pentyn-3-amine, N-butyl-3-methyl-(41040-63-5)
• EPA Substance Registry System: 1-Pentyn-3-amine, N-butyl-3-methyl-(41040-63-5)

Safety Data

• Hazardous Substances Data: 41040-63-5(Hazardous Substances Data)

Usage

Class

The compound belongs to the class of alkynes and amines.

Molar mass

The molar mass of the compound is 155.28 g/mol.

Structure

The compound is made up of a pentyn-3-amine group, which consists of a five-carbon chain with a triple bond and an amino group attached to the third carbon.

Substituent

The compound has a N-butyl-3-methyl moiety, which refers to a butyl group (four-carbon chain) attached to the amino group with a methyl group (one carbon) attached to the third carbon atom of the butyl chain.

Potential uses

The compound has the potential to be used in various synthetic reactions and may have industrial applications.

Upstream product

• 1185-96-2 3-acetoxy-3-ethylbutyne 
• 109-73-9 N-butylamine 
• 77-75-8 meparfynol 
• 10575-70-9 1-bromo-3-methyl-1,2-pentadiene 

Relevant articles and documents

An unprecedented Pd-catalyzed, water-promoted sequential oxidative aminocarbonylation-cyclocarbonylation process leading to 2-oxazolidinones

An unprecedented, Pdl2-catalyzed, sequential oxidative aminocarbonylation-cyclocarbonylation process, leading to 2-oxazolidinone derivatives 3 in good to excellent yields starting from readily available α,α-disubstituted 2-ynylamines 1 and secondary amines 2, is reported. In the case of an α-monosubstituted substrate, the initially formed 2-oxazolidinone derivative underwent shift of the double bond to give a 3H-oxazol-2-one derivative in excellent isolated yield.

Copper Catalyzed Aminolysis of Bromoallenes as a New Efficient Route to Propargylamines

An efficient procedure of general applicability for the synthesis of secondary and tertiary propargylamines by copper mediated aminolysis of 1-bromo-1,2-dienes is described.Key Words: propargylamines; bromoallenes; aminolysis; regioselectivity; Cu promote