105427-51-8

Basic information

• Product Name: 1-Propanamine, 3-methoxy-N-(phenylmethylene)-
• CAS NO: 105427-51-8
• Molecular Formula: C11H15NO
• Molecular Weight: 177.246
• Mol File: 105427-51-8.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 1-Propanamine, 3-methoxy-N-(phenylmethylene)-(CAS DataBase Reference)
• NIST Chemistry Reference: 1-Propanamine, 3-methoxy-N-(phenylmethylene)-(105427-51-8)
• EPA Substance Registry System: 1-Propanamine, 3-methoxy-N-(phenylmethylene)-(105427-51-8)

Safety Data

• Hazardous Substances Data: 105427-51-8(Hazardous Substances Data)

Usage

Chemical class

amines

Composition

three carbon atoms

Common uses

synthesis of pharmaceuticals and organic compounds

Derivative

propanamine

Substituents

methoxy group and phenylmethylene group attached to the amine nitrogen atom

Applications

medicinal and organic chemistry

Suitability

as a building block in the preparation of biologically active compounds

Value

specific properties and reactivity make it a valuable tool for researchers and chemists in the development of new drugs and materials.

Upstream product

• 5433-11-4 N-Benzyliden-3-hydroxy-1-propanamin 
• 74-88-4 methyl iodide 
• 100-52-7 benzaldehyde 

Downstream Products

• 5332-73-0 3-methoxypropylamine 
• 1021461-32-4 [Pd(C₆H₄CHN(CH₂)3OCH₃)(P(C₆H₅)3)(OH₂)]⁽¹⁺⁾ 
• 1021461-21-1 [PdCl(C6H4-2-C(H)=NCH2CH2CH2OMe-κ-C1,N)(triphenylphosphine)] 

Relevant articles and documents

Method for preparing amino ether compounds

The invention belongs to the technical field of organic synthesis and relates to a method for preparing amino ether compounds. The method comprises the following steps: by taking amino alcohol as a raw material, protecting amino in the amino alcohol so as to obtain Schiff base; carrying out an etherification reaction on the hydroxyl group in the Schiff base; and finally, performing amino deprotection, thereby obtaining corresponding amino ethers. The method disclosed by the invention has high regio-selectivity, the substrates of higher than 99.9% are subjected to etherification reaction, the reaction conversion ratio of each step is higher than 99.8%, and the total yield is higher than 95%; when amino alcohol is chiral, the amino ethers with retention of configuration can be obtained; and moreover, each step of the method is a conventional operation, the process cost is low, and three wastes are few, the energy consumption is low, an environment-friendly effect is achieved, and large-scale industrial production is easily realized.