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2-BROMO-5-METHYLBENZOIC ACID

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2-BROMO-5-METHYLBENZOIC ACID Basic information

Product Name:
2-BROMO-5-METHYLBENZOIC ACID
Synonyms:
  • 4-Bromo-3-carboxytoluene, 6-Bromo-m-toluic acid
  • 2-BroMo-5-Methylbenzoic Acid, 97+%
  • 2-Bromo-5-methylbenzoicacid,98%
  • 2-BROMO-5-METHYLBENZOIC ACID
  • NSC20686
  • Benzoic acid,2-bromo-5-methyl-
  • 2-Bromo-5-methylbenzoic Acid >
  • 2-Bromo-5-methylbenzoicaci
CAS:
6967-82-4
MF:
C8H7BrO2
MW:
215.04
Product Categories:
  • Aromatic Carboxylic Acids, Amides, Anilides, Anhydrides & Salts
  • Benzoic acid
  • Acids & Esters
  • Bromine Compounds
Mol File:
6967-82-4.mol
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2-BROMO-5-METHYLBENZOIC ACID Chemical Properties

Melting point:
136-140 °C
Boiling point:
311.6±30.0 °C(Predicted)
Density 
1.599±0.06 g/cm3(Predicted)
storage temp. 
Sealed in dry,Room Temperature
solubility 
Chloroform (Slightly), Methanol (Slightly)
pka
2.92±0.10(Predicted)
form 
Solid
color 
White to Off-White
InChI
InChI=1S/C8H7BrO2/c1-5-2-3-7(9)6(4-5)8(10)11/h2-4H,1H3,(H,10,11)
InChIKey
ZXMISUUIYPFORW-UHFFFAOYSA-N
SMILES
C(O)(=O)C1=CC(C)=CC=C1Br
CAS DataBase Reference
6967-82-4(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xi,Xn
Risk Statements 
36/37/38-22
Safety Statements 
26-36/37/39-37
RIDADR 
UN 2811 6.1 / PGIII
WGK Germany 
3
HazardClass 
IRRITANT
HS Code 
29163990
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2-BROMO-5-METHYLBENZOIC ACID Usage And Synthesis

Chemical Properties

Off-white powder

Synthesis

2941-78-8

6967-82-4

The general procedure for the synthesis of 2-bromo-5-methylbenzoic acid from 2-amino-5-methylbenzoic acid was as follows: CuSO4-5H2O (2.82 g, 11.3 mmol), NaBr (2.31 g, 22.4 mmol), and copper scrapings (1.50 g, 23.6 mmol) were boiled in 15 mL of 47% hydrobromic acid until the solution became colorless. Under heating conditions, 5-methyl-phthalamic acid (5.00 g, 33.1 mmol) was dissolved in a solvent mixture of 11.3 mL of 47% aqueous hydrobromic acid and 28 mL of water. The solution was slowly added to the above CuBr solution at 100°C. The temperature of the reaction mixture was maintained at 90-95°C and 25 mL of aqueous solution of NaNO2 (4.53 g, 65.7 mmol) was slowly added with stirring. Upon completion of the reaction, the precipitated acid was collected by diafiltration, washed with 10% aqueous hydrobromic acid and reprecipitated by adding concentrated hydrochloric acid to the alkaline solution. The crude product was treated by activated charcoal and recrystallized from water three times to give 4.00 g (18.6 mmol, 56% yield) of white crystals with melting point of 137-139°C (literature value: 137.6-139°C). The product was analyzed by IR, 1H NMR, 13C NMR and mass spectrometry to confirm the structure, and the results of elemental analyses were consistent with the theoretical values.

References

[1] Phosphorus, Sulfur and Silicon and the Related Elements, 2015, vol. 190, # 12, p. 2142 - 2153
[2] Journal of Organic Chemistry, 1960, vol. 25, p. 1016 - 1020

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