189079-77-4

Basic information

• Product Name: 1-Butanone, 4-azido-1-(4-chlorophenyl)-
• CAS NO: 189079-77-4
• Molecular Formula: C10H10ClN3O
• Molecular Weight: 223.662
• Mol File: 189079-77-4.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 1-Butanone, 4-azido-1-(4-chlorophenyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: 1-Butanone, 4-azido-1-(4-chlorophenyl)-(189079-77-4)
• EPA Substance Registry System: 1-Butanone, 4-azido-1-(4-chlorophenyl)-(189079-77-4)

Safety Data

• Hazardous Substances Data: 189079-77-4(Hazardous Substances Data)

Upstream product

• 29480-09-9 1-(4-chlorophenyl)cyclobutan-1-ol 
• 40877-09-6 4-chloro-1-(4-chlorophenyl)butan-1-one 

Downstream Products

• 189079-90-1 4,4-Dibromo-5-(4-chloro-phenyl)-3,4-dihydro-2H-pyrrole 
• 189079-86-5 4,4-Dichloro-5-(4-chloro-phenyl)-3,4-dihydro-2H-pyrrole 
• 38944-14-8 2-(4-chlorophenyl)pyrrolidine 
• 22217-78-3 5-(4-chlorophenyl)-3,4-dihydro-2H-pyrrole 

Relevant articles and documents

Synthesis of 3-halopyrroles

3-Chloro- and 3-bromo-2-arylpyrroles, which are potential physiologically active compounds in agrochemistry and pharmaceutical sciences, were efficiently prepared from the corresponding 2-aryl-1-pyrrolines by α,α-dihalogenation with N-halosuccinimides and

Hammett correlation of nornicotine analogues in the aqueous aldol reaction: Implications for green organocatalysis

(Chemical Equation Presented) A series of meta- and para-substituted 2-arylpyrrolidines were synthesized and examined for their ability to catalyze an aqueous aldol reaction under buffered conditions. Kinetic analysis of arylpyrrolidine-catalyzed reactions displayed a linear Hammett correlation with ρ = 1.14 (R2 = 0.996), indicating that the reaction is accelerated by electron-withdrawing aryl rings. These results show promise for the development of a synthetically viable aqueous organocatalyst.