14321-26-7

Basic information

• Product Name: benzyl(methyl)(oxiran-2-ylmethyl)amine
• Synonyms: benzyl(methyl)(oxiran-2-ylmethyl)amine
• CAS NO: 14321-26-7
• Molecular Formula: C₁₁H₁₅NO
• Molecular Weight: 177.2429
• Mol File: 14321-26-7.mol
• Article Data: 5

Chemical Properties

• Appearance: /
• CAS DataBase Reference: benzyl(methyl)(oxiran-2-ylmethyl)amine(CAS DataBase Reference)
• NIST Chemistry Reference: benzyl(methyl)(oxiran-2-ylmethyl)amine(14321-26-7)
• EPA Substance Registry System: benzyl(methyl)(oxiran-2-ylmethyl)amine(14321-26-7)

Safety Data

• Hazardous Substances Data: 14321-26-7(Hazardous Substances Data)

Upstream product

• 103-67-3 benzyl-methyl-amine 
• 106-89-8 epichlorohydrin 
• 3132-64-7 1,2-Epoxy-3-bromopropane 

Downstream Products

• 5431-42-5 1,3-bis-(benzyl-methyl-amino)-propan-2-ol 
• 1404453-52-6 1-[3-(benzylmethylamino)-2-hydroxypropyl]-3-hydroxy-1-methylpyrrolidinium bromide 
• 1100836-00-7 (+/-)-1-[N-benzyl-N-methylamino]-3-[3-thieno[2,3-d]isoxazol-3-yl-phenoxy]-2-propanol 
• 63887-73-0 1-Benzylamino-3-(N-benzylmethylamino)-propan-2-ol 
• 139978-20-4 1-(Benzyl-methyl-amino)-3-(3,3,4,4,5,5,6,6,6-nonafluoro-hexylamino)-propan-2-ol 
• 91595-85-6 2-amino-5-(N-benzyl-N-methylaminomethyl)-2-oxazoline 

Relevant articles and documents

Regio- And Diastereoselective Synthesis of 2-Arylazetidines: Quantum Chemical Explanation of Baldwin's Rules for the Ring-Formation Reactions of Oxiranes ?

A general, scalable two-step regio- and diastereoselective method has been described for the synthesis of versatile alkaloid-type azetidines from simple building blocks with excellent overall yields. In the kinetically controlled reaction, only the format

TRIMERIC MACROCYCLICALLY SUBSTITUTED BENZENE DERIVATIVES

The invention relates to the metal complexes of general formula (I), wherein Hal represents bromine or iodine, and A1 and A2 have different meanings. The inventive metal complexes are suitable for use as contrast media.

2-Amino-2-oxazolines, V: Synthesis of some 5-dialkylaminomethyl-2-amino-2-oxazolines and evaluation of their diuretic activity.

A series of 5-dialkylaminomethyl-2-amino-2-oxazolines was prepared and screened for diuretic activity. These compounds were previously examined for their lipophilic behaviour using a reversed-phase HPLC technique. The capacity factors, expressed as log k'w, were correlated with the partition coefficient log P. A QSAR analysis of the diuretic activity in relation with the lipophilicity was attempted for these structurally related compounds.