15441-95-9

Basic information

• Product Name: N'-(3-Chlorophenyl)-N,N-diethylurea
• Synonyms: N'-(3-Chlorophenyl)-N,N-diethylurea;3-(3-CHLOROPHENYL)-1,1-DIETHYLUREA
• CAS NO: 15441-95-9
• Molecular Formula: C₁₁H₁₅ClN₂O
• Molecular Weight: 226.7
• Mol File: 15441-95-9.mol
• Article Data: 3

Chemical Properties

• Melting Point: 89.5-90 °C
• Boiling Point: 379.2±34.0 °C(Predicted)
• Appearance: /
• Density: 1.185±0.06 g/cm3(Predicted)
• PKA: 14.42±0.70(Predicted)
• CAS DataBase Reference: N'-(3-Chlorophenyl)-N,N-diethylurea(CAS DataBase Reference)
• NIST Chemistry Reference: N'-(3-Chlorophenyl)-N,N-diethylurea(15441-95-9)
• EPA Substance Registry System: N'-(3-Chlorophenyl)-N,N-diethylurea(15441-95-9)

Safety Data

• Hazardous Substances Data: 15441-95-9(Hazardous Substances Data)

Upstream product

• 88-10-8 N,N-diethylcarbamyl chloride 
• 108-42-9 3-chloro-aniline 
• 109-89-7 diethylamine 
• 2909-38-8 m-chlorophenyl isocyanate 
• 20915-05-3 O-(m-Chlorphenyl-carbamoyl)-N_.N-diaethyl-hydroxylamin 
• 21092-83-1 O-(m-Chlorphenyl-carbamoyl)-N-Methyl-N-acetyl-hydroxyl-amin 

Downstream Products

• 1783-38-6 N-(m-Chlorphenyl)-N'.N'-diaethyl-formamidin 

Relevant articles and documents

Synthesis of 2,4-diaminoquinazoline derivatives

A series of 6- and 7-substituted derivatives of 2-(N,N-diethylamino)-4-(N,N-dimethylamino)quinazoline have been synthesized. The synthesis consists in converting N-phenyl-N',N'-diethylurea into chloroamidines which are treated with N,N-dimethylcyanamide t

Process for the preparation of trisubstituted ureas

The present invention provides a process for preparing a trisubstituted urea of the general formula: in which R is a substituted or unsubstituted mono-, di- or polyvalent aromatic radical, R' is a substituted or unsubstituted monovalent aliphatic or aromatic radical and R is a substituted or unsubstituted monovalent aliphatic radical or R' and R together represent a substituted or unsubstituted divalent radical in which at least one of the two carbon atoms adjoining the nitrogen atom of the urea is aliphatic, and n is an integer, wherein an aromatic nitrocompound of the general formula:--R(NO2)n or an aromatic nitrosocompound of the general formula:--R(NO)n is allowed to react with a secondary ammonium N,N-disubstituted thiolcarbamate of the general formula: or with a mixture of a secondary amine of the general formula:--R'R NH and carbon monoxide and sulphur, carbon monoxide and hydrogen sulphide, or carbonyl sulphide, or with a mixture of a secondary ammonium sulphide or hydrosulphide of the general formula: or and carbon monoxide.