4888-74-8

Basic information

• Product Name: 1,3-Propanediamine, 1-phenyl-
• CAS NO: 4888-74-8
• Molecular Formula: C9H14N2
• Molecular Weight: 150.224
• Mol File: 4888-74-8.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 1,3-Propanediamine, 1-phenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: 1,3-Propanediamine, 1-phenyl-(4888-74-8)
• EPA Substance Registry System: 1,3-Propanediamine, 1-phenyl-(4888-74-8)

Safety Data

• Hazardous Substances Data: 4888-74-8(Hazardous Substances Data)

Usage

Physical state

Colorless to pale yellow liquid

Odor

Faint amine odor

Usage

Building block in the synthesis of pharmaceuticals, agrochemicals, and other organic compounds

Intermediate

Production of surfactants and corrosion inhibitors

Applications

Manufacture of polymers and coatings

Safety

Corrosive; can cause skin and eye irritation upon contact

Handling

Handle with care, use appropriate personal protective equipment (PPE) such as gloves, goggles, and face shields.

Upstream product

• 46050-30-0 3-amino-3-phenylpropanamide 
• 74298-71-8 2-Phenyl-pentanedioic acid diamide 
• 3898-37-1 N-(3-Phenyl-n-propyl)sulfamide 
• 15799-07-2 N,N'-Bis-ethoxycarbonyl-1-phenyl-propan-1,3-diamin 
• 936-47-0 5-phenyl-4,5-dihydro-1H-pyrazole 

Downstream Products

• 1308318-28-6 1-(4-bromobenzyl)-5-phenyl-4,5-dihydro-1H-pyrazole 
• 728013-86-3 1-(4-bromobenzyl)-3-phenyl-4,5-dihydro-1H-pyrazole 
• 1308318-16-2 6-(4-bromophenyl)-2-phenyl-1,5-diazabicyclo[3.1.0]hexane 
• 1308318-17-3 2-(4-bromophenyl)-4-phenyl-1,4,5,6-tetrahydropyrimidine 
• 1386980-41-1 N-(5-(3-amino-1-phenylpropylcarbamoyl)-2-chlorophenyl)-2-methoxy-4-methyl-7-oxo-7,8-dihydropyrido[2,3-d]pyrimidine-6-carboxamide 
• 1387089-87-3 N-(5-(3-amino-1-phenylpropylcarbamoyl)-2-chlorophenyl)-2-methyl-7-oxo-7,8-dihydropyrido[2,3-d]pyrimidine-6-carboxamide 
• 1386979-73-2 2-methoxy-7-oxo-7,8-dihydro-pyrido[2,3-d]pyrimidine-6-carboxylic acid [5-(3-amino-1-phenyl-propylcarbamoyl)-2-chloro-phenyl]-amide 
• 208655-12-3 (S)-1-phenyl-1,3-propanediamine 
• 78533-60-5 (4-Phenyl-1,4,5,6-tetrahydro-pyrimidin-2-yl)-carbamic acid isopropyl ester 
• 78533-55-8 2-methoxycarbonylamino-4-phenyl-1,4,5,6-tetrahydropyrimidine 
• 78534-25-5 4-Phenyl-1,4,5,6-tetrahydro-pyrimidin-2-ylamine; hydrobromide 

Relevant articles and documents

Transition-metal-free Intramolecular C-H amination of sulfamate esters and: N -alkylsulfamides

The transition-metal-free intramolecular C-H amination of sulfamate esters using iodine oxidants, tert-butyl hypoiodite (t-BuOI) and N-iodosuccinimide (NIS) is reported. A method using NIS was also successfully applied to the oxidative cyclization of N-alkylsulfamides.

Preparation and Spectroscopic Studies of Stereoisomers of the Triscobalt(III) Complex

Three, fac-Δ, fac-Λ, and mer-Δ, of four possible diastereomers of the 3+ complex (S-phtn=(S)-1-phenyl-1,3-propanediamine) were obtained by two methods, a reaction between trans-+ and S-phtn in DMSO (dimethyl sulfoxide), and oxidation of a DMSO solution containing Co(II) ions and S-phtn with air in the presence of active charcoal.Neither method yielded the mer-Λ isomer.The absorption and circular dichroism spectra of the isomers were recorded in water in the absence and presence of Na2SO4, and in DMSO.The shifts of the first absorption bands caused by changing solvents and the changes of circular dichroism spectra caused by the addition of sulfate ions seem to be related with the conformational instability of the flexible six-membered chelate ring in the complexes.The tetraammine complex of S-phtn was also prepared.