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315-31-1

315-31-1 Structure

315-31-1 Structure
IdentificationMore
[Name]

2-Fluoro-3-methylbenzoic acid
[CAS]

315-31-1
[Synonyms]

2-FLUORO-3-METHYLBENZOIC ACID
2-Fluoro-3-methylbenzoic acid 98%
2-Fluoro-3-methylbenzoicacid98%
[Molecular Formula]

C8H7FO2
[MDL Number]

MFCD00042504
[Molecular Weight]

154.14
[MOL File]

315-31-1.mol
Chemical PropertiesBack Directory
[Melting point ]

114-116
[Boiling point ]

258.4±20.0 °C(Predicted)
[density ]

1.258±0.06 g/cm3(Predicted)
[storage temp. ]

Sealed in dry,Room Temperature
[form ]

powder to crystal
[pka]

3.34±0.10(Predicted)
[color ]

White to Almost white
[InChI]

InChI=1S/C8H7FO2/c1-5-3-2-4-6(7(5)9)8(10)11/h2-4H,1H3,(H,10,11)
[InChIKey]

DGNAETGARNTCIL-UHFFFAOYSA-N
[SMILES]

C(O)(=O)C1=CC=CC(C)=C1F
[CAS DataBase Reference]

315-31-1(CAS DataBase Reference)
Questions And AnswerBack Directory
[Uses]

2-Fluoro-3-methylbenzoic acid is a benzoic acid compound with the general physicochemical properties of benzoic acids. It is mainly used as an intermediate in organic synthesis and can be used to prepare derivatives such as acyl chlorides and amides.
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319-H335
[Precautionary statements ]

P261-P280a-P304+P340-P305+P351+P338-P405-P501a
[Hazard Codes ]

Xi
[Risk Statements ]

22
[Hazard Note ]

Irritant
[HS Code ]

2916399090
Hazard InformationBack Directory
[Chemical Properties]

off white powder
[Synthesis]

1-Arylbenziodoxolones (0.1 mmol), CH2Cl2 (1 mL), and CF3COOH (100 L) were placed in a Schlenk flask. The reaction mixture was stirred for 1 min at room temperature, and then the solvent was evaporated, and the residue was dried under vacuum. CsF (0.3 mmol, 0.1 mmol), TEMPO (0.1 mmol), and dry DMF (500 L) were added to the residue under an argon atmosphere. The reaction mixture was stirred for 20-30 min at 130-150 C. Then water (3 mL or 5% NaHCO3) and CH2Cl2 (3 mL) were added to the reaction mixture. The organic layer was discarded, and HCl (100 L, 37%) and CH2Cl2 (3mL) were added to the water layer. The mixture was shaken for a minute, and then the organic layer was separated, dried with Na2SO4, and the solvent was evaporated. Finally, product 2-Fluoro-3-methylbenzoic acid was obtained after purification.
2-Fluoro-3-methylbenzoic acid
Spectrum DetailBack Directory
[Spectrum Detail]

2-Fluoro-3-methylbenzoic acid(315-31-1)1HNMR
Well-known Reagent Company Product InformationBack Directory
[Sigma Aldrich]

315-31-1(sigmaaldrich)
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