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701-16-6

701-16-6 Structure

701-16-6 Structure
IdentificationBack Directory
[Name]

5-FLUORO-2-METHYLBENZOXAZOLE
[CAS]

701-16-6
[Synonyms]

fluoromethylbenzoxazole
5-FLUORO-2-METHYLBENZOXAZOLE
5-Fluoro-2-methylbenzo[d]oxazole
5-FLUORO-2-METHYLBENZOXAZOLE 97+%
5-Fluoro-2-methyl-1,3-benzoxazole
[Molecular Formula]

C8H6FNO
[MDL Number]

MFCD02093471
[MOL File]

701-16-6.mol
[Molecular Weight]

151.14
Chemical PropertiesBack Directory
[Boiling point ]

90°C 10mm
[density ]

1.23
[refractive index ]

1.5210 to 1.5240
[storage temp. ]

Sealed in dry,Room Temperature
[pka]

1.05±0.10(Predicted)
[Specific Gravity]

1.23
[Appearance]

Yellow to orange Liquid
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H227
[Precautionary statements ]

P501-P210-P280-P370+P378-P403+P235
[Hazard Codes ]

Xn
[Risk Statements ]

36/37/38-22
[Safety Statements ]

26-36/37/39
[TSCA ]

TSCA listed
[HS Code ]

2934999090
Hazard InformationBack Directory
[Uses]

5-Fluoro-2-Methylbenzoxazole is used as a reactant in the preparation of benzothiadiazine compounds as CD73 inhibitors.
[Synthesis]

2-AMINO-4-FLUOROPHENOL

399-97-3

Triethyl orthoacetate

78-39-7

5-FLUORO-2-METHYLBENZOXAZOLE

701-16-6

Procedure for the synthesis of 5-fluoro-2-methylbenzoxazole: 2-amino-4-fluorophenol (1.01 g, 7.95 mmol, 1.0 eq.), triethyl orthoacetate (1.60 mL, 8.7 mmol, 1.1 eq.), and bismuth(III) trifluoromethanesulfonate (50 mg) were mixed and stirred for 30 min at room temperature. Upon completion of the reaction, the reaction mixture was diluted with dichloromethane and purified by rapid chromatography on silica gel (eluent: dichloromethane) to afford 5-fluoro-2-methylbenzoxazole as a clear liquid in a yield of 1.045 g (87% yield). The liquid could be converted to a crystalline solid at lower than 5 °C. Mass spectrum (MALDI-TOF): MH+ = 152. UV/Vis spectrum (methanol): maximum absorption wavelength λmax = 282, 276, 230 nm. 1H NMR (400 MHz, CDCl3): δ 2.60 (s, 3H), 7.02 (1H, td), 7.33 (1H, dd), 7.39 (1H, dd).

[References]

[1] Patent: WO2008/40994, 2008, A2. Location in patent: Page/Page column 25
[2] Patent: WO2017/98421, 2017, A1. Location in patent: Page/Page column 223
Spectrum DetailBack Directory
[Spectrum Detail]

5-FLUORO-2-METHYLBENZOXAZOLE(701-16-6)MS
5-FLUORO-2-METHYLBENZOXAZOLE(701-16-6)1HNMR
5-FLUORO-2-METHYLBENZOXAZOLE(701-16-6)IR1
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