17918-11-5

Basic information

• Product Name: alpha-phenylaziridine-1-ethanol
• Synonyms: alpha-phenylaziridine-1-ethanol;2-aziridin-1-yl-1-phenyl-ethanol;1-Phenyl-2-(1-aziridinyl)ethanol;2-(1-Aziridinyl)-1-phenylethanol;α-Phenyl-1-aziridineethanol
• CAS NO: 17918-11-5
• Molecular Formula: C₁₀H₁₃NO
• Molecular Weight: 163.21632
• EINECS: 241-861-4
• Mol File: 17918-11-5.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 290.31°C (rough estimate)
• Flash Point: 138.1°C
• Appearance: /
• Density: 1.0508 (rough estimate)
• Vapor Pressure: 0.00217mmHg at 25°C
• Refractive Index: 1.5400 (estimate)
• CAS DataBase Reference: alpha-phenylaziridine-1-ethanol(CAS DataBase Reference)
• NIST Chemistry Reference: alpha-phenylaziridine-1-ethanol(17918-11-5)
• EPA Substance Registry System: alpha-phenylaziridine-1-ethanol(17918-11-5)

Safety Data

• Hazardous Substances Data: 17918-11-5(Hazardous Substances Data)

Usage

Safety Profile

Poison by intravenous, intraperitoneal, and intravenous routes. When heated to decomposition it emits toxic fumes of NOx.

InChI:InChI=1/C10H13NO/c12-10(8-11-6-7-11)9-4-2-1-3-5-9/h1-5,10,12H,6-8H2

Upstream product

• 96-09-3 styrene oxide 
• 870-24-6 2-chloroethanamine hydrochloride 
• 17619-22-6 1-ethyleneimine 
• 151-56-4 ethyleneimine 

Downstream Products

• 89446-71-9 2-(2-Methylsulfanyl-ethylamino)-1-phenyl-ethanol 
• 89446-72-0 1-Phenyl-2-(2-propylsulfanyl-ethylamino)-ethanol 
• 78969-64-9 1-(β-Hydroxyphenylethyl)-3-iminothiazolidine hydrochloride 
• 89446-74-2 2-(2-Butylsulfanyl-ethylamino)-1-phenyl-ethanol 
• 133760-85-7 2-hydroxy-2-phenyl-N-(2-phenylthioethyl)ethylamine 
• 89446-73-1 N-β-Isopropylthioethyl-2-hydroxy-2-phenylethyl amine 
• 89446-75-3 2-(2-Benzylsulfanyl-ethylamino)-1-phenyl-ethanol 
• 17899-33-1 2-imino-3-(2'-hydroxy-2'-phenylethyl)thiazolidine hydrochloride 
• 17899-26-2 1-(2'-acetoxy-2'-phenylethyl)aziridine 
• 7568-93-6 2-Amino-1-phenylethanol 
• 46189-96-2 α-<(2-Bromethylamino)-methyl>-benzylalkohol 
• 33449-10-4 2-[2-(N-Methyl-hydrazino)-ethylamino]-1-phenyl-ethanol 
• 20405-97-4 3-(2-hydroxy-2-phenyl-ethyl)-thiazolidin-2-one 

Relevant articles and documents

Regioselective synthesis of N-β-hydroxyethylaziridines by the ring-opening reaction of epoxides with aziridine generated in situ

Biologically important N-β-hydroxyethylaziridine intermediates were conveniently prepared by regioselective ring-opening reactions of diversely substituted epoxides. Ethyleneimine generated in situ under basic conditions from β-chloroethylamine was used a

Method of preparing dl 6-phenyl-2,3,5,6-tetrahydroimidazo-[2,1-b]thiazole and acid addition salts thereof

An improved method of preparing acid addition salts of dl 6-phenyl-2,3,5,6-tetrahydroimidazo[2,1-b]thiazole (dl-tetramisole) by reacting dl-3-(β-hydroxyphenethyl)-2-iminothiazolidine or an acid-addition salt thereof, with a mixture of concentrated hydroch