79322-24-0

Basic information

• Product Name: 1-phenyl-3-trimethylaminopropyl carbodiimide
• Synonyms: 1-phenyl-3-trimethylaminopropyl carbodiimide
• CAS NO: 79322-24-0
• Molecular Formula: C₁₃H₂₀N₃*I
• Molecular Weight: 0
• Mol File: 79322-24-0.mol
• Article Data: 3

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 1-phenyl-3-trimethylaminopropyl carbodiimide(CAS DataBase Reference)
• NIST Chemistry Reference: 1-phenyl-3-trimethylaminopropyl carbodiimide(79322-24-0)
• EPA Substance Registry System: 1-phenyl-3-trimethylaminopropyl carbodiimide(79322-24-0)

Safety Data

• Hazardous Substances Data: 79322-24-0(Hazardous Substances Data)

Usage

InChI:InChI=1/C13H20N3.HI/c1-16(2,3)11-7-10-14-12-15-13-8-5-4-6-9-13;/h4-6,8-9H,7,10-11H2,1-3H3;1H/q+1;/p-1

Upstream product

• 103-71-9 phenyl isocyanate 
• 109359-63-9 (3-Dimethylamino-propyl)-phosphoramidic acid diethyl ester 
• 109-55-7 1-amino-3-(dimethylamino)propane 
• 32022-55-2 1-(3-Dimethylamino-propyl)-3-phenyl-urea 
• 79322-23-9 1-phenyl-3-(3-(dimethylamino)propyl)carbodiimide 
• 74-88-4 methyl iodide 

Relevant articles and documents

Substituent effects in the addition of carboxylic acids to arylcarbodiimides

Rates of addition in aqueous solution of RCOOH (R = CH3-, CH3OCH2-, ClCH2-, Cl2CH-) to ArN=C=NCH2-CH2CH2N+(CH3) 3 [Ar = C6H

Preparation of Carbodiimides Using Phase-Transfer Catalysis

A new method is described for the preparation of carbodiimides by dehydration of ureas with arenesulfonyl chlorides under solid-liquid phase-transfer catalytic (PTC) conditions using solid potassium carbonate as a base and a lipophilic quaternary ammonium salt as a catalyst.The method is generally applicable for the synthesis of disubstituted carbodiimides, but is especially useful for unsymmetrically substituted carbodiimides.The basic carbodiimides prepared were identified in the form of the more stable, crystalline quaternary salts.