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94087-40-8

94087-40-8 Structure

94087-40-8 Structure
IdentificationMore
[Name]

3-Chloro-2-fluorobenzonitrile
[CAS]

94087-40-8
[Synonyms]

2-FLUORO-3-CHLOROBENZONITRILE
3-CHLORO-2-FLUOROBENZONITRILE
BUTTPARK 45\01-06
[EINECS(EC#)]

301-934-4
[Molecular Formula]

C7H3ClFN
[MDL Number]

MFCD00042206
[Molecular Weight]

155.56
[MOL File]

94087-40-8.mol
Chemical PropertiesBack Directory
[Appearance]

white to light yellow crystal powder
[Melting point ]

40-44 °C(lit.)
[Boiling point ]

206.3±20.0 °C(Predicted)
[density ]

1.33±0.1 g/cm3(Predicted)
[Fp ]

164 °F
[storage temp. ]

Sealed in dry,Room Temperature
[solubility ]

soluble in Methanol
[form ]

powder to lump
[color ]

White to Light yellow to Light orange
[InChI]

InChI=1S/C7H3ClFN/c8-6-3-1-2-5(4-10)7(6)9/h1-3H
[InChIKey]

CHKLNKWJIDQKFV-UHFFFAOYSA-N
[SMILES]

C(#N)C1=CC=CC(Cl)=C1F
[CAS DataBase Reference]

94087-40-8(CAS DataBase Reference)
[NIST Chemistry Reference]

Benzonitrile, 3-chloro-2-fluoro-(94087-40-8)
Safety DataBack Directory
[Hazard Codes ]

Xn,T,Xi,N
[Risk Statements ]

R20/21/22:Harmful by inhalation, in contact with skin and if swallowed .
[Safety Statements ]

S36/37:Wear suitable protective clothing and gloves .
[RIDADR ]

3439
[WGK Germany ]

3
[Hazard Note ]

Toxic
[HazardClass ]

6.1
[HazardClass ]

IRRITANT
[PackingGroup ]

III
[HS Code ]

29269090
[Storage Class]

11 - Combustible Solids
[Hazard Classifications]

Acute Tox. 4 Dermal
Acute Tox. 4 Inhalation
Hazard InformationBack Directory
[Chemical Properties]

white to light yellow crystal powder
[Synthesis]

2,3-Dichlorobenzonitrile

6574-97-6

3-Chloro-2-fluorobenzonitrile

94087-40-8

General procedure for the synthesis of 3-chloro-2-fluorobenzonitrile from 2,3-dichlorobenzonitrile: Under the protection of nitrogen, 1200g of cyclobutanesulfone, 280g of potassium fluoride, 50g of tetramethylammonium chloride and 688g of 2,3-dichlorobenzonitrile were added to a dry 2L four-necked flask. stirring was turned on, and the temperature was slowly raised to 210°C and kept at this temperature for 8 hours, and the progress of the reaction was monitored by a control sample until the The content of the reaction material was ≤1%. After the reaction was completed, the reaction solution was subjected to short distillation, and 560 g of 2-fluoro-3-chlorobenzonitrile was collected, with the product purity ≥99% and the yield of 90%.

[References]

[1] Patent: CN104529729, 2016, B. Location in patent: Paragraph 0025; 0026
[2] Angewandte Chemie - International Edition, 2006, vol. 45, # 17, p. 2720 - 2725
Spectrum DetailBack Directory
[Spectrum Detail]

3-Chloro-2-fluorobenzonitrile(94087-40-8)1HNMR
3-Chloro-2-fluorobenzonitrile(94087-40-8)IR
Well-known Reagent Company Product InformationBack Directory
[Sigma Aldrich]

94087-40-8(sigmaaldrich)
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