64980-40-1

Basic information

• Product Name: 2-Propanol, 1-[(1,1-dimethylethyl)amino]-3-phenoxy-
• CAS NO: 64980-40-1
• Molecular Formula: C13H21NO2
• Molecular Weight: 223.315
• Mol File: 64980-40-1.mol
• Article Data: 14

Chemical Properties

• CAS DataBase Reference: 2-Propanol, 1-[(1,1-dimethylethyl)amino]-3-phenoxy-(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Propanol, 1-[(1,1-dimethylethyl)amino]-3-phenoxy-(64980-40-1)
• EPA Substance Registry System: 2-Propanol, 1-[(1,1-dimethylethyl)amino]-3-phenoxy-(64980-40-1)

Safety Data

• Hazardous Substances Data: 64980-40-1(Hazardous Substances Data)

Upstream product

• 122-60-1 Phenyl glycidyl ether 
• 75-64-9 tert-butylamine 
• 108-95-2 phenol 
• 119072-55-8 tert-butylisonitrile 
• 2120-70-9 2-phenoxyethanal 
• 192652-08-7 C₂₂H₂₂O₃ 
• 122-99-6 2-Phenoxyethanol 
• 56-23-5 tetrachloromethane 
• 1746-13-0 allyl phenyl ether 
• 74953-47-2 N-tert-Butyl-2-hydroxy-3-phenoxy-propionamide 
• 766-94-9 vinyl phenyl ether 
• 50381-48-1 trioxo(N-tert-butylimido)osmium(VIII) 

Relevant articles and documents

Crystal packing of alcohol amines formed by the reaction of primary amines with 1,2-epoxy-3-phenoxypropane

For the purposes of characterizing a novel class of inorganic-organic hybrid epoxy resin materials, a series of amines were reacted with a monoepoxide (1,2-epoxy-3-phenoxypropane) under base catalyzed conditions to produce racemic mixtures of compounds wi

CONTINUOUS FLOW SYNTHESIS OF AMINO ALCOHOLS USING MICROREACTORS

The present invention provides various methods for the synthesis of chemical species in a microreactor environment. In some cases, reaction products of the present invention may be valuable as intermediates and/or products in pharmaceutical and polymer research. For example, the method may involve the synthesis of amino alcohols within a microchannel. Embodiment described herein may allow for reactions with significantly shorter reaction times and increased efficiency.

Metallocene catalyzed synthesis of fungistatic vicinal aminoalcohols under solvent free conditions

Group 4 and 5 metallocenes, Cp2TiCl2, Cp 2ZrCl2 and Cp2VCl2, have been evaluated as catalyst in the solvent free, room temperature, preparation of vicinal aminoalcohols. The regioselectivity of the reaction and the fungistatic activity of the prepared compounds against Botrytis cinerea and Colletotrichum gloeosporioides are discussed.