Basic information Uses Safety Supplier Related
ChemicalBook >  Product Catalog >  Organic Chemistry >  Alcohols,Phenols,Phenol alcohols >  Phenol derivatives >  4-Bromo-2-methoxyphenol

4-Bromo-2-methoxyphenol

Basic information Uses Safety Supplier Related

4-Bromo-2-methoxyphenol Basic information

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
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
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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)
Flash point:
>230 °F
storage temp. 
Inert atmosphere,Room Temperature
solubility 
Chloroform, Methanol
pka
9.40±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 Reference
7368-78-7(CAS DataBase Reference)
NIST Chemistry Reference
4-Bromoguaiacol(7368-78-7)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-36
WGK Germany 
3
Hazard Note 
Irritant
HS Code 
29095000

MSDS

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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.

Uses

It is an important raw material and intermediate used in organic synthesis, pharmaceuticals, agrochemicals and dyestuff.

Uses

4-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.

4-Bromo-2-methoxyphenol Preparation Products And Raw materials

Raw materials

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