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4-fluoro-3-(trifluoromethyl)benzonitrile

4-fluoro-3-(trifluoromethyl)benzonitrile

CAS: 67515-59-7

Molecular Formula: C8H3F4N

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4-fluoro-3-(trifluoromethyl)benzonitrile - Names and Identifiers

Name 4-fluoro-3-(trifluoromethyl)benzonitrile
Synonyms BUTTPARK 451-76
5-CYANO-2-FLUOROBENZOTRIFLUORIDE
à,à,à,4-tetrafluoro-m-tolunitrile
3-Trifluoromethyl-4-fluorobenzonitrile
4-Fluoro-3-Trifluoromethylbenzonitrile
4-Fluoro-3-(Trifluromethyl)Benzonitrile
4-Fluoro-3-(trifluoromethyl)benzonitrile
3-(TRIFLUOROMETHYL)-4-FLUOROBENZONITRILE
4-fluoro-3-(trifluoromethyl)benzonitrile
4-FLUORO-3-(TRIFLUOROMETHYL)BENZONITRILE
4-Fluoro-3-Trifluoromethylbenzonitrile 3-Trifluoromethyl-4-fluorobenzonitrile
5-Cyano-2-fluorobenzotrifluoride~alpha,alpha,alpha,4-Tetrafluoro-m-tolunitrile
CAS 67515-59-7
InChI InChI=1/C8H3F4N/c9-7-2-1-5(4-13)3-6(7)8(10,11)12/h1-3H

4-fluoro-3-(trifluoromethyl)benzonitrile - Physico-chemical Properties

Molecular FormulaC8H3F4N
Molar Mass189.11
Density1,323 g/cm
Melting Point66 °C
Boling Point194°C
Flash Point193-195°C
Water SolubilityInsoluble in water.
Vapor Presure0.291mmHg at 25°C
BRN1960344
Storage ConditionSealed in dry,Room Temperature
Refractive Index1.443

4-fluoro-3-(trifluoromethyl)benzonitrile - Risk and Safety

Risk CodesR20/21/22 - Harmful by inhalation, in contact with skin and if swallowed.
R36/37/38 - Irritating to eyes, respiratory system and skin.
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.
S45 - In case of accident or if you feel unwell, seek medical advice immediately (show the label whenever possible.)
S36 - Wear suitable protective clothing.
S36/37 - Wear suitable protective clothing and gloves.
S23 - Do not breathe vapour.
S9 - Keep container in a well-ventilated place.
UN IDs3276
HS Code29269090
Hazard NoteToxic
Hazard Class6.1
Packing GroupIII

4-fluoro-3-(trifluoromethyl)benzonitrile - Reference Information

Introduction 4-fluoro-3-trifluoromethylbenzonitrile is a 3-trifluoromethyl 4-halobenzonitrile compound. 3-Trifluoromethyl 4-halobenzonitrile is an important component of many dyes, herbicides, pharmaceuticals and natural compounds, and is also an important organic synthesis intermediate. Its cyano group can be converted into ketone, amide, carboxylic acid, imine ester, carboxylic acid ester, thioamide and a series of compounds.
preparation 10 mmol of 3-trifluoromethyl -4-haloaniline is dissolved in 10mL of micro-hot glacial acetic acid, 2.5 mL of 12
mol · L-1 sulfuric acid solution is slowly added, stirred and dissolved into burnt yellow solution, then cooled to 0~5 in an ice salt bath, and stirred into white paste, then drop 10ml
2mol · L-1 NaNO2 solution cooled to 0~5 ℃ into white paste (about 30 min )
to form red-brown diazonium salt solution until the starch potassium iodide test paper test solution is blue, and finally neutralize glacial acetic acid with Na2CO3 to pH = 7.0. It is directly used in the synthesis of the target compound
without separation and precipitation. Dissolve 0.84g(2 mmo1) K3[Fe(CN)6] in 20mL of distilled water, add 4.5mmol ethylenediamine and 1.5 mmolCu
(OAc)2 to it, stir for 1 h at room temperature, then transfer to an ice salt bath and cool to 0-5 ℃. The above diazonium salt solution was added dropwise to K3[Fe(CN)6] solution (about 1
h), and stirred continuously for 2 h under the cooling of ice salt bath, resulting in reddish brown precipitation. The precipitate is filtered out, the solid is washed with dichloromethane, the organic phase is collected, the aqueous phase is extracted with 1/3 volume of dichloromethane twice, the organic phase is collected,
and the organic phase is combined twice, the column is concentrated under reduced pressure, and the product is separated by elution (petroleum ether: ethyl acetate = 20:1).
use for pharmaceutical intermediates
Last Update:2024-04-09 02:00:02
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4-fluoro-3-(trifluoromethyl)benzonitrile
3,5-Dimethyl-2,6-dibromopyridine
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