65875-39-0

Basic information

• Product Name: 1,2-Ethanediamine, N'-[(4-methoxyphenyl)methyl]-N,N-dimethyl-
• CAS NO: 65875-39-0
• Molecular Formula: C12H20N2O
• Molecular Weight: 208.304
• Mol File: 65875-39-0.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 1,2-Ethanediamine, N'-[(4-methoxyphenyl)methyl]-N,N-dimethyl-(CAS DataBase Reference)
• NIST Chemistry Reference: 1,2-Ethanediamine, N'-[(4-methoxyphenyl)methyl]-N,N-dimethyl-(65875-39-0)
• EPA Substance Registry System: 1,2-Ethanediamine, N'-[(4-methoxyphenyl)methyl]-N,N-dimethyl-(65875-39-0)

Safety Data

• Hazardous Substances Data: 65875-39-0(Hazardous Substances Data)

Usage

Category

Chemical compound

Function

Antihistamine and anticholinergic medication

Medical Uses

Treats allergic reactions, hay fever, and pruritus (itching)

Mechanism of Action

Blocks the effects of histamine, a substance that causes allergy symptoms

Administration

Typically administered orally or topically

Onset of Action

Relatively rapid

Side Effects

May cause drowsiness and other central nervous system side effects

Precautions

Should be used with caution in individuals operating heavy machinery or vehicles

Dosage

Follow dosing instructions provided by a healthcare professional

Upstream product

• 2393-23-9 4-methoxy-benzylamine 
• 107-99-3 2-(dimethylamino)ethyl chloride 
• 3717-21-3 p-methoxyl benzaldoxime 
• 86154-87-2 (2-chloro-ethyl)-(4-methoxy-benzyl)-amine 
• 124-40-3 dimethyl amine 
• 91907-70-9 N'-(4-methoxy-benzylidene)-N,N-dimethyl-ethylenediamine 

Downstream Products

• 553-13-9 Zolamine 
• 91-85-0 thonzylamine 
• 96588-34-0 N',N'-Dimethyl-N-<4-methoxy-benzyl>-N-fluorenyl-(9)-aethylendiamin 
• 91-84-9 pyrilamine 

Relevant articles and documents

Photoredox-catalyzed decarboxylative cross-coupling of α-amino acids with nitrones

A decarboxylative cross-coupling reaction of α-amino acids with nitrones via visible-light-induced photoredox catalysis has been established for easy access to β-amino hydroxylamines and vicinal diamines with structural diversity, which is featured with simple operation, mild conditions, readily available α-amino acids, and a broad scope of nitrone substrates. The application of this protocol can furnish efficient synthetic strategies for some valuable vicinal diamine-containing molecules.