Basic information Safety Supplier Related

4-BROMOMETHYL-3-FLUOROBENZOIC ACID METHYL ESTER

Basic information Safety Supplier Related

4-BROMOMETHYL-3-FLUOROBENZOIC ACID METHYL ESTER Basic information

Product Name:
4-BROMOMETHYL-3-FLUOROBENZOIC ACID METHYL ESTER
Synonyms:
  • 4-(bromomethyl)-3-fluorobenzoic acid
  • Methyl 4-broMoMethyl-3-fluorobenzoate
  • Methyl 4-bromomethyl-3-fluorobenzoat
  • -3-fluorobenzoate
  • 4-BROMOMETHYL-3-FLUOROBENZOIC ACID METHYL
  • 4-BROMOMETHYL-3-FLUOROBENZOIC ACID METHYL ESTER
  • MMETHYL 4-(BROMOMETHYL)-3-FLUOROBENZOATE
  • Benzoicacid, 4-(bromomethyl)-3-fluoro-, methyl ester
CAS:
128577-47-9
MF:
C9H8BrFO2
MW:
247.06
EINECS:
604-604-1
Mol File:
128577-47-9.mol
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4-BROMOMETHYL-3-FLUOROBENZOIC ACID METHYL ESTER Chemical Properties

Melting point:
68 °C(Solv: ethyl ether (60-29-7); hexane (110-54-3))
Boiling point:
295.1±35.0 °C(Predicted)
Density 
1.534±0.06 g/cm3(Predicted)
storage temp. 
under inert gas (nitrogen or Argon) at 2-8°C
form 
solid
color 
White
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Safety Information

HS Code 
2916399090
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4-BROMOMETHYL-3-FLUOROBENZOIC ACID METHYL ESTER Usage And Synthesis

Uses

Methyl 4-(bromomethyl)-3-fluorobenzoate

Synthesis

87808-48-8

128577-47-9

Bromination reaction: Methyl 3-fluoro-4-methylbenzoate (18.3 mmol) was dissolved with N-bromosuccinimide (NBS, 3.9 g, 22 mmol) in carbon tetrachloride (40 mL), and benzoyl peroxide (0.55 g, 1.7 mmol) containing 25% water was added as initiator. The reaction mixture was stirred well and heated to reflux for 6 hours. Upon completion of the reaction, the solvent was removed by evaporation and the residue was treated with an aqueous solution of potassium carbonate (K2CO3) followed by extraction of the product with ethyl acetate (EtOAc). After treatment, methyl 3-fluoro-4-(bromomethyl)benzoate was obtained as a light yellow solid in a yield of 5.9 g. The product was analyzed by electrospray ionization mass spectrometry (ESI-MS), which showed the [M + H]+ peak as 247 Da.

References

[1] Patent: WO2014/102376, 2014, A1. Location in patent: Page/Page column 45
[2] Patent: WO2014/102377, 2014, A1. Location in patent: Page/Page column 49-50
[3] Journal of Medicinal Chemistry, 2015, vol. 58, # 15, p. 6058 - 6080
[4] Synlett, 2014, vol. 25, # 17, p. 2485 - 2487
[5] Patent: US2006/14945, 2006, A1. Location in patent: Page/Page column 60

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