3-Bromo-5-hydroxypyridine
3-Bromo-5-hydroxypyridine Basic information
- Product Name:
- 3-Bromo-5-hydroxypyridine
- Synonyms:
-
- 3-BROMO-5-HYDROXYPYRIDINE 98.5+%
- 3-Hydro-5-broMo-pyridin
- 5-Bromopyridine-3-ol
- 3--5- hydroxypyridiniuMbroMide
- 3-BroMo-5-hydroxypyridine, 97+%
- 3-Bromo-5-hydroxypyridine 97%
- 5-BROMO-3-PYRIDINOL
- 5-BROMO-3-HYDROXYPYRIDINE
- CAS:
- 74115-13-2
- MF:
- C5H4BrNO
- MW:
- 174
- EINECS:
- 627-764-3
- Product Categories:
-
- pharmacetical
- Pyridines, Pyrimidines, Purines and Pteredines
- Building Blocks
- Halogenated
- Chemical Amines
- Aromatics
- Amines
- blocks
- Bromides
- Heterocycles
- Boronic Acid
- C5Heterocyclic Building Blocks
- Halogenated Heterocycles
- Heterocyclic Building Blocks
- Pyridines
- Pyridine
- Pyridine Series
- Mol File:
- 74115-13-2.mol
3-Bromo-5-hydroxypyridine Chemical Properties
- Melting point:
- 166-170 °C
- Boiling point:
- 343.7±22.0 °C(Predicted)
- Density
- 1.788±0.06 g/cm3(Predicted)
- storage temp.
- Inert atmosphere,Room Temperature
- solubility
- DMSO (Slightly), Methanol (Slightly)
- pka
- 8.37±0.10(Predicted)
- form
- Crystalline Powder
- color
- White to tan
- Water Solubility
- Slightly soluble in water. Soluble in chloroform and ethyl acetate.
- InChI
- InChI=1S/C5H4BrNO/c6-4-1-5(8)3-7-2-4/h1-3,8H
- InChIKey
- VNYBIBSZZDAEOK-UHFFFAOYSA-N
- SMILES
- C1=NC=C(Br)C=C1O
- CAS DataBase Reference
- 74115-13-2(CAS DataBase Reference)
Safety Information
- Hazard Codes
- Xi,Xn
- Risk Statements
- 36/37/38-22-20/21/22
- Safety Statements
- 26-36/37/39-37-36-22
- WGK Germany
- 3
- HazardClass
- IRRITANT
- HS Code
- 29339900
3-Bromo-5-hydroxypyridine Usage And Synthesis
Description
3-bromo-5-hydroxypyridine is an important industrial raw material widely used in medicine, pesticides, dyes, and other industries. Since the pyridine ring has biological activity and plays an irreplaceable role in synthesising drugs that cannot be replaced by other groups or functional groups, it is a hot area in pharmaceutical research. The hydroxyl and bromine atoms in the structure of 3-bromo-5-hydroxypyridine have diverse chemical reactivity. The alcohol hydroxyl unit in its structure can undergo nucleophilic substitution reactions with common alkyl halides under alkaline conditions to obtain corresponding ether derivatives.
Chemical Properties
Light yellow needles
Uses
5-Bromo-3-methoxypyridine was refluxed with 20 mL (57%) of hydrogen bromide for 24 hours. The reaction was quenched with saturated sodium bicarbonate solution and the base mixture was extracted with 3 × 50 mL of dichloromethane. The organic fractions were pooled, dried (magnesium sulfate), filtered, and evaporated to give a white solid (3 g, >95% purity) identified as 3-bromo-5-hydroxypyridine by thin layer chromatography.
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3-Bromo-5-hydroxypyridine(74115-13-2)Related Product Information
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