83004-10-8

Basic information

• Product Name: 2-BROMO-6-(BROMOMETHYL)PYRIDINE
• Synonyms: PYRIDINE, 2-BROMO-6-(BROMOMETHYL)-;2-BROMO-6-(BROMOMETHYL)PYRIDINE;6-Bromo-2-bromomethylpyridine
• CAS NO: 83004-10-8
• Molecular Formula: C₆H₅Br₂N
• Molecular Weight: 250.92
• Product Categories: Heterocycle-Pyridine series
• Mol File: 83004-10-8.mol
• Article Data: 24

Chemical Properties

• Boiling Point: 275℃
• Flash Point: 120℃
• Appearance: /
• Density: 1.955
• Vapor Pressure: 0.009mmHg at 25°C
• Refractive Index: 1.613
• Storage Temp.: under inert gas (nitrogen or Argon) at 2-8°C
• PKA: -1.00±0.12(Predicted)
• CAS DataBase Reference: 2-BROMO-6-(BROMOMETHYL)PYRIDINE(CAS DataBase Reference)
• NIST Chemistry Reference: 2-BROMO-6-(BROMOMETHYL)PYRIDINE(83004-10-8)
• EPA Substance Registry System: 2-BROMO-6-(BROMOMETHYL)PYRIDINE(83004-10-8)

Safety Data

• HazardClass: IRRITANT
• Hazardous Substances Data: 83004-10-8(Hazardous Substances Data)

Usage

General Description

2-Bromo-6-(bromomethyl)pyridine is a compound that contains two bromine atoms attached to a pyridine ring, with one of the bromine atoms being attached to a methyl group. This chemical is commonly used in the synthesis of pharmaceuticals and agrochemicals. It is a versatile building block for creating complex organic molecules, particularly those with biological activity. The presence of bromine atoms on the pyridine ring can impart specific chemical properties to the compound, making it suitable for a range of applications in the pharmaceutical and agricultural industries. However, it is important to handle this chemical with care due to its potential hazards and toxicity.

InChI:InChI=1/C6H5Br2N/c7-4-5-2-1-3-6(8)9-5/h1-3H,4H2

Upstream product

• 5315-25-3 2-bromo-6-methylpyridine 
• 33674-96-3 2-bromo-6-(hydroxymethyl)pyridine 
• 1824-81-3 2-Amino-6-methylpyridine 

Downstream Products

• 83004-11-9 1-(6-bromopyridin-2-yl)-N,N-dimethylmethanamine 
• 882426-55-3 dibenzyl-[2-(6-bromo-pyridin-2-ylmethoxy)-1,1-bis-(6-bromo-pyridin-2-ylmethoxymethyl)-ethyl]-amine 
• 958880-85-8 (6-bromo-pyridin-2-ylmethyl)-cyclohexylmethyl-(2-trifluoromethyl-benzyl)-amine 
• 1010086-53-9 tert-butyl cis-1-((6-bromopyridin-2-yl)methyl)-4-((tert-butyl(diphenyl)silyl)oxy)cyclohexanecarboxylate 
• 882426-56-4 C₅₁H₆₂N₄O₉ 
• 112575-11-8 2-(6-bromopyridin-2-yl)acetonitrile 
• 937265-89-9 1-(6-bromo-pyridin-2-ylmethyI)-3-(3,4-dimethyl-benzoyl)-1H-quinolin-4-one 
• 1192575-01-1 N-[(6-bromopyridin-2-yl)methoxy]-1-(4-methyl-4H-1,2,4-triazol-3-yl)-1-phenylmethanimine 
• 1187833-88-0 N-[(6-bromopyridin-2-yl)methoxy]-1-(1-methyl-1H-tetrazol-5-yl)-1-phenylmethanimine 
• 1206455-34-6 C₁₈H₁₄Br₂N₄O₄S 
• 1192224-51-3 2-(6-bromopyridin-2-ylmethyl)-6-(3,5-difluorophenyl)-2H-pyridazin-3-one 
• 1429913-28-9 benzyl {6-[(2-hydroxy-2-methylpropoxy)methyl]pyridin-2-yl}carbamate 

Relevant articles and documents

Ruthenium complexes bearing unsymmetric CNC' pincer ligands: Molecular structures and electronic properties

Homoleptic ruthenium complexes [Ru(Ln)2]2+ bearing unsymmetric pyridine-based bis N-heterocyclic carbene (NHC) pincer ligands are synthesized and structurally characterized. These complexes feature the coexistence of a five-membered and a six-membered ruthenacycle within the same ligand framework, allowing an ideally octahedral CNHC-Ru-N Py bite angle close to 90°. In the solid state, impressive 3MLCT lifetimes of microsecond regime were detected in all of the complexes, of which [Ru(L4)2]2+, featuring four benzimidazol-2-ylidene donors, exhibited the longest values. Electronic properties of all of the ruthenium complexes are investigated by cyclic voltammetry and spectroscopic techniques. Density functional theory results were used to support the experimental observations.

Ruthenium complexes bearing N-heterocyclic carbene based CNC and CN^CH2C’ pincer ligands: Photophysics, electrochemistry, and solar energy conversion

A combination of N-heterocyclic carbene (NHC) based CNC, or CN^CH2C′ pincer ligands and carboxy-phenyl terpyridine donors is used to prepare ruthenium complexes. The unsymmetrical coordination of CN^CH2C′ pincer

HETEROCYCLIC COMPOUND AND USE THEREOF

The present invention provides a heterocyclic compound having an orexin type 2 receptor agonist activity. A compound represented by the formula (I) : wherein each symbol is as described in the specification, or a salt thereof, is useful as an agent for the prophylaxis treatment of narcolepsy.

Tri-(2-picolyl)amine-modificated triarylborane: Synthesis, photophysical properties and distinguish for cyanide and fluoride anions in aqueous solution

We designed and synthesized a tri-(2-picolyl) amine (TPA) functionalized triarylborane, 1-(6-(4-(dimesitylboryl)phenyl)pyridin-2-yl)-N,N-bis(pyridin-2-ylmethyl)methanamine (PB2). The photophysical properties of PB2 were thoroughly explored. Moreover, PB2