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ChemicalBook--->CAS DataBase List--->153556-42-4

153556-42-4

153556-42-4 Structure

153556-42-4 Structure
IdentificationMore
[Name]

4-Bromo-3-fluorobenzoic acid
[CAS]

153556-42-4
[Synonyms]

4-BROMO-3-FLUOROBENZOIC ACID
BUTTPARK 20\01-57
3-Fluoro-4-Bromo Benzoic Acid
4-Bromo-3-fluorobenzoic
4-Bromo-3-fluorobenzoic acid, 98+%
[EINECS(EC#)]

630-193-2
[Molecular Formula]

C7H4BrFO2
[MDL Number]

MFCD00672932
[Molecular Weight]

219.01
[MOL File]

153556-42-4.mol
Chemical PropertiesBack Directory
[Melting point ]

207 °C
[Boiling point ]

296.1±25.0 °C(Predicted)
[density ]

1.789±0.06 g/cm3(Predicted)
[storage temp. ]

Sealed in dry,Room Temperature
[form ]

powder
[pka]

3.63±0.10(Predicted)
[color ]

Off white to cream
[InChI]

InChI=1S/C7H4BrFO2/c8-5-2-1-4(7(10)11)3-6(5)9/h1-3H,(H,10,11)
[InChIKey]

RMYOGXPGIDWJLU-UHFFFAOYSA-N
[SMILES]

C(O)(=O)C1=CC=C(Br)C(F)=C1
[CAS DataBase Reference]

153556-42-4(CAS DataBase Reference)
[EPA Substance Registry System]

Benzoic acid, 4-bromo-3-fluoro- (153556-42-4)
Safety DataBack Directory
[Hazard Codes ]

Xi
[Risk Statements ]

R36/37/38:Irritating to eyes, respiratory system and skin .
[Safety Statements ]

S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S36/37/39:Wear suitable protective clothing, gloves and eye/face protection .
[Hazard Note ]

Irritant
[HazardClass ]

IRRITANT
[HS Code ]

2916399090
Hazard InformationBack Directory
[Chemical Properties]

White solid powder
[Uses]

4-Bromo-3-fluorobenzoic acid is an important chemical raw material and can be used to prepare a variety of drugs (such as the anticancer drug benzamide).
[Synthesis]

4-Bromo-3-fluorotoluene

452-74-4

4-Bromo-3-fluorobenzoic acid

153556-42-4

The general procedure for the synthesis of 3-fluoro-4-bromobenzoic acid from 3-fluoro-4-bromotoluene was as follows: potassium permanganate (66.0 g, 0.42 mol) was added to a mixed solution of pyridine and water (1:1 ratio, 200 mL) containing 1-bromo-2-fluoro-4-methylbenzene (20.0 g, 0.10 mol) in batches. The reaction mixture was stirred at 90 °C for 3 hours. After completion of the reaction, it was cooled to room temperature and filtered through a diatomaceous earth pad. The diatomaceous earth pad was washed sequentially with 3N sodium hydroxide solution (500 mL) and water (400 mL). Subsequently, ethanol was removed by distillation under reduced pressure and the residue was acidified to pH=2 with 6N hydrochloric acid to produce a white precipitate. The precipitate was filtered and dried to give 4-bromo-3-fluorobenzoic acid as a white solid (17.0 g, 73% yield).

[References]

[1] Bioorganic and Medicinal Chemistry Letters, 2001, vol. 11, # 10, p. 1257 - 1260
[2] Journal of Medicinal Chemistry, 2003, vol. 46, # 14, p. 2973 - 2984
[3] Patent: WO2011/21209, 2011, A1. Location in patent: Page/Page column 38
[4] Patent: US2012/101099, 2012, A1. Location in patent: Page/Page column 13; 14
[5] Patent: WO2006/64251, 2006, A1. Location in patent: Page/Page column 80
Spectrum DetailBack Directory
[Spectrum Detail]

4-Bromo-3-fluorobenzoic acid(153556-42-4)FT-IR
Well-known Reagent Company Product InformationBack Directory
[Alfa Aesar]

4-Bromo-3-fluorobenzoic acid, 98+%(153556-42-4)
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