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3-Fluoro-4-methylphenol

3-Fluoro-4-methylphenol

CAS: 452-78-8

Molecular Formula: C7H7FO

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3-Fluoro-4-methylphenol - Names and Identifiers

Name 3-Fluoro-4-methylphenol
Synonyms QR CF D1
452-78-8
QR CF D1 [WLN]
3-FLUORO-P-CRESOL
3-Fluoro-p-cresol
3-FLUORO-4-METHYLPHENOL
3-Fluoro-4-methylphenol
2-Fluoro-4-hydroxytoluene
Phenol, 3-fluoro-4-methyl
phenol, 3-fluoro-4-methyl-
Phenol, 3-fluoro-4-methyl-
3-Fluoro-4-methylphenol, JRD,
CAS 452-78-8
EINECS 200-110-4
InChI InChI=1/C7H7FO/c1-5-2-3-6(9)4-7(5)8/h2-4,9H,1H3

3-Fluoro-4-methylphenol - Physico-chemical Properties

Molecular FormulaC7H7FO
Molar Mass126.13
Density1.17
Melting Point72 °C
Boling Point196 °C
Flash Point29 °C
Vapor Presure0.32mmHg at 25°C
AppearanceYellow solid
pKa9.27±0.18(Predicted)
Storage ConditionInert atmosphere,Room Temperature
SensitiveSensitive to air
Refractive Index1.5150
MDLMFCD00143164
Physical and Chemical PropertiesPale yellow oily liquid

3-Fluoro-4-methylphenol - Risk and Safety

Risk CodesR21/22 - Harmful in contact with skin and if swallowed.
R34 - Causes burns
R52 - Harmful to aquatic organisms
R36 - Irritating to the eyes
R22 - Harmful if swallowed
Safety DescriptionS26 - 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.
S60 - This material and its container must be disposed of as hazardous waste.
S45 - In case of accident or if you feel unwell, seek medical advice immediately (show the label whenever possible.)
UN IDs2922
HS Code29081990
Hazard NoteIrritant
Hazard Class8

3-Fluoro-4-methylphenol - Reference Information

Application 3-fluoro-4-methylphenol can be used as intermediates in organic synthesis and pharmaceutical intermediates, mainly used in laboratory research and development process and chemical production process.
preparation 5-methoxy-2-methylaniline (5.0g,36mmol), A mixture of hydrochloric acid (7.6ml of
12M solution, 91mmol) and water (11ml) was heated at 60 °c for 15 minutes until complete
dissolution. The reaction mixture was cooled to 0 °c and an aqueous solution of NaNO2(2.5g,36mmol) was added dropwise (internal temperature <7 °c). The reaction mixture was stirred at 0 °c for 30 minutes and a 0 °c solution of
HBF4 (48% ml of a 1.2 solution, 40mmol) was carefully added. The reaction mixture was stirred at 0 °c for 20 minutes and the brown solid formed was filtered off and washed with ice water (3 x 10ml) and water (2 x 10ml). The solid was dried under high vacuum for 20 hours and then heated (air heat gun) until
BF3 (white smoke) evolution ceased. The resulting brown oil was partitioned between ethyl acetate and water. The organic phase was dried (Na2SO4), concentrated under reduced pressure, and distilled with Kugelrohr tube distiller to give 3-fluoro-4-methylanisole (1.6g,31%), it is a colorless oil. To a solution of 3-fluoro-4-methylanisole (1.62g,11.6mmol) in CH2Cl2(10ml)
at -70 °c was added dropwise BBr3(10ml, 12mmol). The reaction mixture was stirred at -70 °c for 10 minutes, then warmed to 0 °c and stirred at 0 °c for 2 hours. It was then warmed to room temperature, concentrated under reduced pressure and the residue partitioned between water and EtOAc. The organic phase was washed with water, dried over Na2SO4 and concentrated under reduced pressure to give 3-fluoro-4-methylphenol (1.1g,75%),
as an oil.
Chemical properties light yellow oily liquid
Last Update:2024-04-09 19:05:05
3-Fluoro-4-methylphenol
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View History
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