181647-50-7

Basic information

• Product Name: (5-BROMO-PYRIDIN-2-YL)-PHENYL-METHANOL
• Synonyms: (5-BROMO-PYRIDIN-2-YL)-PHENYL-METHANOL;(5-Bromo-2-pyridyl)-phenyl-methanol
• CAS NO: 181647-50-7
• Molecular Formula: C₁₂H₁₀BrNO
• Molecular Weight: 264.12
• Mol File: 181647-50-7.mol
• Article Data: 4

Chemical Properties

• Appearance: /
• CAS DataBase Reference: (5-BROMO-PYRIDIN-2-YL)-PHENYL-METHANOL(CAS DataBase Reference)
• NIST Chemistry Reference: (5-BROMO-PYRIDIN-2-YL)-PHENYL-METHANOL(181647-50-7)
• EPA Substance Registry System: (5-BROMO-PYRIDIN-2-YL)-PHENYL-METHANOL(181647-50-7)

Safety Data

• Hazardous Substances Data: 181647-50-7(Hazardous Substances Data)

Usage

General Description

(5-BROMO-PYRIDIN-2-YL)-PHENYL-METHANOL is a chemical compound with the molecular formula C12H10BrNO. It consists of a phenyl group attached to a pyridine ring with a bromine atom at the 5th position and a hydroxyl group attached to the phenyl group. (5-BROMO-PYRIDIN-2-YL)-PHENYL-METHANOL is used in the synthesis of pharmaceuticals, agrochemicals, and other organic compounds. It has potential applications in the field of medicinal chemistry and drug development. Additionally, it can be used as a building block in organic synthesis to create more complex molecules. Overall, (5-BROMO-PYRIDIN-2-YL)-PHENYL-METHANOL has a variety of potential uses in the chemical and pharmaceutical industries due to its unique structure and reactivity.

Upstream product

• 624-28-2 2,5-dibromopyridine 
• 119-61-9 benzophenone 
• 100-52-7 benzaldehyde 

Downstream Products

• 1374992-34-3 (5-bromopyridin-2-yl)(phenyl)methyl 2.2,2-trichloroethanimidoate; 
• 1227862-76-1 (5-(4-nitrophenyl)pyridin-2-yl)(phenyl)methanol 
• 1613186-56-3 6-bromo-3-phenyl-[1,2,3]triazolo[1,5-a]pyridine 
• 1613186-51-8 [(5-bromopyridin-2-yl)phenylmethylene]hydrazone 
• 206357-52-0 (5-bromopyridin-2-yl)(phenyl)methanone 

Relevant articles and documents

Regioselective Bromine/Magnesium Exchange for the Selective Functionalization of Polyhalogenated Arenes and Heterocycles

Using the bimetallic combination sBu2Mg?2 LiOR (R=2-ethylhexyl) in toluene enables efficient and regioselective Br/Mg exchanges with various dibromo-arenes and -heteroarenes under mild reaction conditions and provides bromo-substituted magnesiu

Selective monolithiation of 2,5-dibromopyridine with butyllithium

Selective monolithiation of 2,5-dibromopyridine at either the 2-position or the 5-position is reported. Solvent and concentration strongly influence the selectivity. Coordinating solvents and higher concentration favor the 5- position while non-coordinati