Basic information Safety Supplier Related

3-BROMO-4-HYDROXYPHENYLACETIC ACID

Basic information Safety Supplier Related

3-BROMO-4-HYDROXYPHENYLACETIC ACID Basic information

Product Name:
3-BROMO-4-HYDROXYPHENYLACETIC ACID
Synonyms:
  • 3-BROMO-4-HYDROXYBENZENEACETIC ACID
  • 3-BROMO-4-HYDROXYPHENYLACETIC ACID
  • 3-Bromo-4-hydroxyphenyl
  • 2-(3-bromo-4-hydroxyphenyl)acetic acid
  • Benzeneacetic acid, 3-bromo-4-hydroxy-
CAS:
38692-80-7
MF:
C8H7BrO3
MW:
231.04
EINECS:
254-089-8
Product Categories:
  • Aromatic Phenylacetic Acids and Derivatives
  • Organic acids
Mol File:
38692-80-7.mol
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3-BROMO-4-HYDROXYPHENYLACETIC ACID Chemical Properties

Melting point:
105-107℃
Boiling point:
364℃
Density 
1.757
Flash point:
174℃
storage temp. 
Sealed in dry,Room Temperature
pka
4.33±0.10(Predicted)
CAS DataBase Reference
38692-80-7(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xi,Xn
Risk Statements 
22
HazardClass 
IRRITANT
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3-BROMO-4-HYDROXYPHENYLACETIC ACID Usage And Synthesis

Synthesis

774-81-2

38692-80-7

Step (b) 3-bromo-4-methoxyphenylacetic acid (14.0 g, 0.057 mol) and anhydrous dichloromethane (100 mL) were added to a 250 mL round bottom flask. The reaction mixture was degassed by nitrogen bubbling for 5 min. Subsequently, a dichloromethane solution of 1 M boron tribromide (63 mL, 0.063 mol) was added slowly and dropwise through the addition funnel. The reaction mixture was stirred at room temperature and a white solid was observed to precipitate gradually. After the reaction was carried out for 2 h, the product was separated by filtration and the collected white crystals were washed several times with dichloromethane to finally obtain 3-bromo-4-hydroxyphenylacetic acid (12 g, 92% yield).

References

[1] Patent: US2003/114457, 2003, A1
[2] Patent: WO2004/62661, 2004, A1. Location in patent: Page/Page column 28
[3] Patent: US2009/197959, 2009, A1. Location in patent: Page/Page column 14; 15

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