161417-28-3

Basic information

• Product Name: 4-BROMO-3-HYDROXYPYRIDINE
• Synonyms: 4-BROMO-3-HYDROXYPYRIDINE;4-BROMO-3-PYRIDINOL;4-BROMO-3-HYDROXYOPYRIDINE;4-Bromopyridin-3-ol;4-boro-3-hydroxypyridine;3-Pyridinol, 4-bromo-
• CAS NO: 161417-28-3
• Molecular Formula: C₅H₄BrNO
• Molecular Weight: 174
• EINECS: -0
• Product Categories: Pyridines, Pyrimidines, Purines and Pteredines;pharmacetical;Pyridine;Chemical Amines;Amines;Aromatics;Heterocycles;Pyridines
• Mol File: 161417-28-3.mol
• Article Data: 3

Chemical Properties

• Melting Point: 134-136°C
• Boiling Point: 316.2 °C at 760 mmHg
• Flash Point: 145 °C
• Appearance: White solid
• Density: 1.788 g/cm³
• Vapor Pressure: 0.000225mmHg at 25°C
• Refractive Index: 1.614
• Storage Temp.: -20°C Freezer
• Solubility: Chloroform (Sparingly), Ethyl Acetate
• PKA: 6.57±0.10(Predicted)
• CAS DataBase Reference: 4-BROMO-3-HYDROXYPYRIDINE(CAS DataBase Reference)
• NIST Chemistry Reference: 4-BROMO-3-HYDROXYPYRIDINE(161417-28-3)
• EPA Substance Registry System: 4-BROMO-3-HYDROXYPYRIDINE(161417-28-3)

Safety Data

• Hazardous Substances Data: 161417-28-3(Hazardous Substances Data)

Usage

Chemical Properties

White Solid

InChI:InChI=1/C5H4BrNO/c6-4-1-2-7-3-5(4)8/h1-3,8H

Upstream product

• 10182-48-6 3,4-dihydroxypyridine 
• 98976-81-9 4-bromo-pyridin-3-yl diethylcarbamate 

Downstream Products

• 882170-26-5 [1-(4-bromo-pyridin-3-yloxymethyl)-2-phenyl-ethyl]-carbamic acid tert-butyl ester 
• 1219102-40-5 acetic acid 4-bromo-pyridin-3-yl ester 
• 193605-52-6 5-chloro-2,3-dihydrofuro[2,3-c]pyridine 
• 19539-50-5 furo<2,3-c>pyridine 
• 1610521-11-3 4-bromo-3-(cyclopropylmethoxy)pyridine 

Relevant articles and documents

Toolbox for regioselective lithiations of furo[2,3-c]pyridine

Chemical Reaction Reprentation A detailed procedure for successive regioselective lithiations of furo[2,3-c]pyridine is described by using n-BuLi and the [n-BuLi/LiDMAE] Superbase. Several polysubstituted furo[2,3-c]pyridines have been efficiently synthesized and some of them were engaged in Pd- or Ni-catalyzed coupling reactions leading to 2,2'- or 7,7'-bifuro[2,3-c]pyridine ligands.

3-pyridyloxymethyl heterocyclic ether compounds useful in controlling neurotransmitter release

Novel heterocyclic ether compounds of the formula: STR1 wherein n, *, R1, R2, R3 and y are specifically defined, or pharmaceutically acceptable salts or prodrugs thereof, which are useful in selectively controlling neurotransmitter release; therapeutically-effective pharmaceutical compositions of these compounds; and use of said compositions to selectively control neurotransmitter release in mammals.