1049706-69-5

Basic information

• Product Name: 2-phenyl-3-nitro-6-chloropyridine
• Synonyms: 2-phenyl-3-nitro-6-chloropyridine
• CAS NO: 1049706-69-5
• Molecular Weight: 234.642
• Mol File: 1049706-69-5.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 2-phenyl-3-nitro-6-chloropyridine(CAS DataBase Reference)
• NIST Chemistry Reference: 2-phenyl-3-nitro-6-chloropyridine(1049706-69-5)
• EPA Substance Registry System: 2-phenyl-3-nitro-6-chloropyridine(1049706-69-5)

Safety Data

• Hazardous Substances Data: 1049706-69-5(Hazardous Substances Data)

Upstream product

• 91678-23-8 2-bromo-6-chloro-3-nitropyridine 
• 98-80-6 phenylboronic acid 
• 134896-35-8 2-phenyl-3-nitropyridine 
• 16013-85-7 2,6-dicholoro-3-nitropyridine 
• 1049706-68-4 3-nitro-2-phenylpyridine N-oxide 

Relevant articles and documents

Organic electroluminescent material and device thereof

Disclosed are an organic electroluminescent material and a device thereof. The organic electroluminescent material is a novel triaryl amine-aza-carbazole quinazoline compound. The compound is used asa host material in an electroluminescent device and prov

Ortho-(Dimesitylboryl)phenylphosphines: Positive boryl effect in the palladium-catalyzed suzuki-miyaura coupling of 2-chloropyridines

Catalytic systems combining ortho-(dimesitylboryl) phenylphosphines and palladium precursors have been evaluated in the Suzuki-Miyaura couplings of chloro-N-heterocycles, in particular 2-chloro pyridines, with arylboronic acids. The Lewis basic character of the substrates does not interfere with the Lewis acidic site of the ligands, even for a substrate featuring free NH2 groups. The influence of several reaction parameters has been studied and the ortho-dimesitylboryl moiety was actually found to substantially enhance the catalytic performance. The role of this group has been examined using preformed phosphine-borane/Pd complexes and the formation of an original phosphine/h4-boratabutadiene complex has been identified as a possible deactivation pathway. Regioselective coupling of 2,6-dichloro-3-nitropyridine with phosphine-borane/Pd catalysts has also been explored, and sequential double cross-couplings were found to give a direct and efficient access to unsymmetrical 2,6-diarylpyridines.