22422-27-1

Basic information

• Product Name: 3-chloro-1-(p-tolyl)propan-1-ol
• Synonyms: 3-chloro-1-(p-tolyl)propan-1-ol
• CAS NO: 22422-27-1
• Molecular Weight: 184.666
• Mol File: 22422-27-1.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 3-chloro-1-(p-tolyl)propan-1-ol(CAS DataBase Reference)
• NIST Chemistry Reference: 3-chloro-1-(p-tolyl)propan-1-ol(22422-27-1)
• EPA Substance Registry System: 3-chloro-1-(p-tolyl)propan-1-ol(22422-27-1)

Safety Data

• Hazardous Substances Data: 22422-27-1(Hazardous Substances Data)

Upstream product

• 22422-21-5 4'-methyl-3-chloropropiophenone 
• 108-88-3 toluene 

Downstream Products

• 22912-91-0 Acetic acid 3-chloro-1-p-tolyl-propyl ester 
• 1352742-03-0 (R)-3-chloro-1-p-tolylpropyl acetate 
• 1037716-92-9 1-(4-methylphenyl)-1-phenoxy-3-chloropropane 
• 1028270-76-9 1-(4-methylphenyl)-1-(2,4-dichlorophenoxy)-3-chloropropane 
• 1037717-03-5 1-(4-methylphenyl)-1-(2,4-dimethylphenoxy)-3-chloropropane 
• 1037716-93-0 1-(4-methylphenyl)-1-(4-chlorophenoxy)-3-chloropropane 
• 1037717-01-3 1-(4-methylphenyl)-1-(2-chloro-4-methylphenoxy)-3-chloropropane 
• 1037717-02-4 1-(4-methylphenyl)-1-(2-methyl-4-chlorophenoxy)-3-chloropropane 
• 1037717-00-2 1-(4-methylphenyl)-1-(3,5-dichlorophenoxy)-3-chloropropane 
• 1037716-98-5 1-(4-methylphenyl)-1-(4-tert-butylphenoxy)-3-chloropropane 
• 1037716-99-6 1-(4-methylphenyl)-1-(2,6-dichlorophenoxy)-3-chloropropane 
• 1037716-97-4 1-(4-methylphenyl)-1-(4-isopropylphenoxy)-3-chloropropane 
• 1037716-96-3 1-(4-methylphenyl)-1-(4-ethylphenoxy)-3-chloropropane 
• 1037716-95-2 1-(4-methylphenyl)-1-(4-methylphenoxy)-3-chloropropane 

Relevant articles and documents

Imidazole analogues of fluoxetine, a novel class of anti-Candida agents

Imidazole analogues of fluoxetine have been obtained by replacing the methylamino terminus of aminopropane chain with the imidazole ring. The newly designed imidazoles showed potent anti-Candida activity, superior to those of miconazole and other antifungal agents of clinical interest. 1-(4-Chlorophenyl)-l-(2,4-dichlorophenoxy)-3-(1H-imidazol-1-yl)propane (16), the most active among test imidazoles, Was about 2-fold more active and as much less cytotoxic than miconazole. High increase of activity was observed with methyl, nitro, fluorine, and chlorine (Cl > F > CH3 > NO2 > CF3).