23281-56-3

Basic information

• Product Name: 1,3-Dimethyl-2-(4-chlorophenyl)imidazolidine
• Synonyms: 1,3-Dimethyl-2-(4-chlorophenyl)imidazolidine;2-(4-Chlorophenyl)-1,3-dimethylimidazolidine
• CAS NO: 23281-56-3
• Molecular Formula: C₁₁H₁₅ClN₂
• Molecular Weight: 210.7032
• Mol File: 23281-56-3.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 267.6°Cat760mmHg
• Flash Point: 115.6°C
• Appearance: /
• Density: 1.126g/cm³
• Vapor Pressure: 0.00809mmHg at 25°C
• Refractive Index: 1.551
• PKA: 6.78±0.40(Predicted)
• CAS DataBase Reference: 1,3-Dimethyl-2-(4-chlorophenyl)imidazolidine(CAS DataBase Reference)
• NIST Chemistry Reference: 1,3-Dimethyl-2-(4-chlorophenyl)imidazolidine(23281-56-3)
• EPA Substance Registry System: 1,3-Dimethyl-2-(4-chlorophenyl)imidazolidine(23281-56-3)

Safety Data

• Hazardous Substances Data: 23281-56-3(Hazardous Substances Data)

Usage

InChI:InChI=1/C11H15ClN2/c1-13-7-8-14(2)11(13)9-3-5-10(12)6-4-9/h3-6,11H,7-8H2,1-2H3

Upstream product

• 104-88-1 4-chlorobenzaldehyde 
• 110-70-3 N,N`-dimethylethylenediamine 

Downstream Products

• 623-27-8 terephthalaldehyde, 
• 52010-95-4 4-(1-hydroxy-1-phenylmethyl)benzaldehyde 
• 102-11-4 N-benzyl-N-methyl-N'-methylethylenediamine 
• 59793-79-2 4-(1-hydroxy-2,2-dimethylpropyl) benzaldehyde 
• 23229-37-0 1,3-dimethyl-2-phenylimidazolidine 
• 162896-87-9 bis-(4,4′-formyl)benzophenone 
• 1571-08-0 methyl 4-formylbenzoate 

Relevant articles and documents

Cyclopentyl methyl ether-NH4X: A novel solvent/catalyst system for low impact acetalization reactions

Cyclopentyl methyl ether, a low impact ether forming a positive azeotrope with water, was successfully employed as a solvent in the synthesis of 1,3-dioxanes and 1,3-dioxolanes carried out under Dean-Stark conditions by the acetalization of aliphatic and aromatic aldehydes or ketones, employing ammonium salts as environmentally friendly acidic catalysts.

Comparative radioprotective activity of various pentagonal compounds with two heteroatomes

Various heterocyclic compounds with two heteroatomes were synthesized and their potential radioprotective activity was tested. This study shows the interest of phenylthiazolidines derivatives in chemical radioprotection.