1301629-37-7

Basic information

• Product Name: 2-azido-1-(2,4-dichlorophenyl)ethan-1-ol
• Synonyms: 2-azido-1-(2,4-dichlorophenyl)ethan-1-ol
• CAS NO: 1301629-37-7
• Molecular Weight: 232.069
• Mol File: 1301629-37-7.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 2-azido-1-(2,4-dichlorophenyl)ethan-1-ol(CAS DataBase Reference)
• NIST Chemistry Reference: 2-azido-1-(2,4-dichlorophenyl)ethan-1-ol(1301629-37-7)
• EPA Substance Registry System: 2-azido-1-(2,4-dichlorophenyl)ethan-1-ol(1301629-37-7)

Safety Data

• Hazardous Substances Data: 1301629-37-7(Hazardous Substances Data)

Upstream product

• 2631-72-3 2,4-dichlorophenacyl bromide 
• 2234-16-4 1-(2,4-dichlorophenyl)ethan-1-one 
• 4252-78-2 2,2',4'-trichloroacetophenone 
• 13692-14-3 α-(chloromethyl)-2,4-dichlorobenzyl alcohol 

Downstream Products

• 1301629-38-8 1-(2-azido-1-(4-chlorobenzyloxy)ethyl)-2,4-dichlorobenzene 
• 1301629-39-9 1-(2-azido-1-(4-(trifluoromethoxy)benzyloxy)ethyl)-2,4-dichlorobenzene 
• 1301629-40-2 1-((2-azido-1-(2,4-dichlorophenyl)ethoxy)methyl)-2,4-difluorobenzene 
• 1301629-30-0 2-(4-butyl-1H-1,2,3-triazol-1-yl)-1-(2,4-dichlorophenyl)ethanol 
• 1301629-31-1 1-(2,4-dichlorophenyl)-2-(4-(2-hydroxyethyl)-1H-1,2,3-triazol-1-yl)ethanol 
• 1301629-27-5 1-(2,4-dichlorophenyl)-2-(4-(hydroxymethyl)-1H-1,2,3-triazol-1-yl)ethanol 
• 1301629-32-2 2-(4-cyclohexyl-[1,2,3]triazol-1-yl)-1-(2,4-dichlorophenyl)ethanol 
• 1301629-33-3 2-(4-tert-butyl-1H-1,2,3-triazol-1-yl)-1-(2,4-dichlorophenyl)ethanol 
• 1301629-34-4 2-(4-(3-aminophenyl)-1H-1,2,3-triazol-1-yl)-1-(2,4-dichlorophenyl)ethanol 
• 1301629-35-5 2-(4-(4-aminophenyl)-1H-1,2,3-triazol-1-yl)-1-(2,4-dichlorophenyl)ethanol 
• 1301629-36-6 1-(2,4-dichlorophenyl)-2-(4-(pyridin-2-yl)-1H-1,2,3-triazol-1-yl)ethanol 
• 1301628-94-3 4-butyl-1-(2-(4-chlorobenzyloxy)-2-(2,4-dichlorophenyl)ethyl)-1H-1,2,3-triazole 
• 1301628-96-5 4-butyl-1-(2-(2,4-dichlorophenyl)-2-(4-(trifluoromethoxy)benzyloxy)ethyl)-1H-1,2,3-triazole 
• 1301628-98-7 4-butyl-1-(2-(2,4-dichlorophenyl)-2-(2,4-difluorobenzyloxy)ethyl)-1H-1,2,3-triazole 

Relevant articles and documents

Carbon isotope labeling of carbamates by late-stage [11C], [13C] and [14C]carbon dioxide incorporation

A general procedure for the late-stage [11C], [13C] and [14C]carbon isotope labeling of cyclic carbamates is reported. This protocol allows the incorporation of carbon dioxide, the primary source of carbon-14 and carbon-11 radioisotopes, in a direct, cost-effective and sustainable manner. A disconnection/reconnection strategy, involving ring opening/isotopic closure, was also implemented.

Design and synthesis of 1H-1,2,3-triazoles derived from econazole as antitubercular agents

Econazole has been known to be active against Mycobacterium tuberculosis. We have designed and synthesized 1H-1,2,3-triazoles derived from econazole as antitubercular agents. The majority of triazole derivatives have been prepared by microwave-assisted cl