4381-32-2

Basic information

• Product Name: Pyridine, 2-(2-chlorophenyl)-
• CAS NO: 4381-32-2
• Molecular Formula: C11H8ClN
• Molecular Weight: 189.644
• Mol File: 4381-32-2.mol
• Article Data: 36

Chemical Properties

• CAS DataBase Reference: Pyridine, 2-(2-chlorophenyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Pyridine, 2-(2-chlorophenyl)-(4381-32-2)
• EPA Substance Registry System: Pyridine, 2-(2-chlorophenyl)-(4381-32-2)

Safety Data

• Hazardous Substances Data: 4381-32-2(Hazardous Substances Data)

Upstream product

• 109-04-6 2-bromo-pyridine 
• 108-90-7 chlorobenzene 
• 1008-89-5 2-phenylpyridine 
• 1448009-89-9 benzo[h]quinoline 
• 98-98-6 2-Picolinic acid 
• 675-20-7 piperidin-2-one 
• 2142-68-9 1-(2-chlorophenyl)ethanone 
• 694-59-7 pyridine N-oxide 
• 694-80-4 2-bromo-1-chlorobenzene 
• 98-80-6 phenylboronic acid 
• 109-09-1 2-chloropyridine 
• 3900-89-8 2-Chlorobenzeneboronic acid 
• 615-41-8 2-iodochlorobenzene 
• 17997-47-6 2-tri-n-butylstannylpyridine 

Downstream Products

• 485385-78-2 2-{2-[2-(trimethylsilyl)ethynyl]phenyl}pyridine 
• 1217887-31-4 C₁₂H₇ClF₃N 
• 1581719-28-9 2-(2-chloro-6-((triisopropylsilyl)ethynyl)phenyl)pyridine 
• 879088-40-1 2-(2-chloro-5-nitrophenyl)-pyridine 
• 879088-41-2 4-chloro-3-(pyridin-2-yl)benzeneamine 
• 879085-55-9 vismodegib 
• 478944-03-5 2-(2-vinylphenyl)pyridine 
• 33421-18-0 2-(2-chlorophenyl)-pyridine-N-oxide 
• 1044209-44-0 C₁₁H₉ClN₂ 
• 4381-30-0 2-(2,5-dichlorophenyl)pyridine 

Relevant articles and documents

Light-promoted C-Cl bond-forming reductive elimination of a metal-metal bonded PdIII-PdIIIcomplex

The excited-state reductive elimination (RE) activities of a metal-metal bonded PdIII2complex, [(2-phenylpyridyl)Pd(μ-acetate)Cl]2, are described. The C-Cl bond-forming RE reaction is accelerated by up to five orders of magnitude upon visible p

Tris-NHC-propagated self-supported polymer-based Pd catalysts for heterogeneous C-H functionalization

Three-dimensionally propagated imidazolium-containing mesoporous coordination polymer and organic polymer-based platforms were successfully exploited to develop single-site heterogenized Pd-NHC catalysts for oxidative arene/heteroarene C-H functionalization reactions. The catalysts were efficient in directed arene halogenation, and nondirected arene and heteroarene arylation reactions. High catalytic activity, excellent heterogeneity and recyclability were offered by these systems making them promising candidates in the area of heterogeneous C-H functionalization, where efficient catalysts are still scarce.

Salen-based hypercrosslinked polymer-supported Pd as an efficient and recyclable catalyst for C-H halogenation

In this work, we report the first use of a salen-based hypercrosslinked polymer-supported Pd catalyst to carry out C-H halogenation. This catalyst can effectively catalyze C-H bromination and chlorination even better than its homogeneous counterpart Pd(OAc)2. It also showed excellent reusability without loss of catalytic activity for ten cycles. A broad substrate scope was explored and moderate to excellent yields were obtained.