4-Bromo-2-methoxyphenol

4-Bromo-2-methoxyphenol
  • CAS No.:7368-78-7
Other grades of this product :
4-Bromo-2-methoxyphenol Basic information
Uses
Product Name:4-Bromo-2-methoxyphenol
Synonyms:4-BROMOGUAIACOL;4-BROMO-2-METHOXYPHENOL;AKOS 225-06;2-Methoxy-4-Bromophenol;4-Bromo-2-methoxyphenol,4-Bromoguaiacol;4-Bromo-2-methoxyphenol 98%;4-Bromoguaiacol, 5-Bromo-2-hydroxyanisole;B**4-Bromoguaiacol
CAS:7368-78-7
MF:C7H7BrO2
MW:203.03
EINECS:
Product Categories:Building Blocks;C6 to C8;Chemical Synthesis;Organic Building Blocks;Oxygen Compounds;Phenols;blocks;Bromides;Benzene series;Miscellaneous
Mol File:7368-78-7.mol
4-Bromo-2-methoxyphenol Chemical Properties
Melting point 34-37 °C (lit.)
Boiling point 129-132°C 12mm
density 1.585±0.06 g/cm3(Predicted)
Fp >230 °F
storage temp. Inert atmosphere,Room Temperature
solubility Chloroform, Methanol
pka9.40±0.18(Predicted)
form Low Melting Solid or Crystalline Solid
color Colorless to white to pale brown
Water Solubility Slightly soluble in water.
BRN 2045286
CAS DataBase Reference7368-78-7(CAS DataBase Reference)
NIST Chemistry Reference4-Bromoguaiacol(7368-78-7)
Safety Information
Hazard Codes Xi
Risk Statements 36/37/38
Safety Statements 26-36
WGK Germany 3
Hazard Note Irritant
HS Code 29095000
MSDS Information
ProviderLanguage
SigmaAldrich English
ALFA English
4-Bromo-2-methoxyphenol Usage And Synthesis
Uses

4-bromo-2-methoxyphenol is an important organic intermediate (building block) to synthetize substituted phenzyl products, and it can also be used for the synthesis of polyfunctionalized bicyclic systems.

UsesIt is an important raw material and intermediate used in organic synthesis, pharmaceuticals, agrochemicals and dyestuff.
Uses4-Bromo-2-methoxyphenol is an important raw material and intermediate used in organic synthesis, pharmaceuticals, agrochemicals and dyestuff.A. Schoenberg; R. F. Heck. Palladium-catalyzed formylation of aryl, heterocyclic, and vinylic halides. J. Am. Chem. Soc. 1974, 96 (25), 7761-7764.Joel S. Freundlich; Howard E. Landis. An expeditious aqueous Suzuki-Miyaura method for the arylation of bromophenols. Tetrahedron Letters. 2006, 47(25), 4275-4279.

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