Cas no 93343-11-4 (2,4,6-Trifluorotoluene)

2,4,6-Trifluorotoluene structure
2,4,6-Trifluorotoluene structure
Product Name:2,4,6-Trifluorotoluene
CAS No:93343-11-4
MF:C7H5F3
MW:146.109812498093
MDL:MFCD04039204
CID:821182
Update Time:2023-10-12

2,4,6-Trifluorotoluene Chemical and Physical Properties

Names and Identifiers

    • 2,4,6-TRIFLUOROTOLUENE
    • 2,3-DIHYDROXY-DL-PHENYLALANINE
    • 2,4,6-Trifluorotolune
    • 2-Methyl-1,3,5-trifluorobenzene
    • 1,3,5-Trifluoro-2-methylbenzene (ACI)
    • 2,4,6-Trifluorotoluene
    • MDL: MFCD04039204
    • Inchi: 1S/C7H5F3/c1-4-6(9)2-5(8)3-7(4)10/h2-3H,1H3
    • InChI Key: HZCVONJWZPKKBI-UHFFFAOYSA-N
    • SMILES: FC1C=C(F)C(C)=C(F)C=1

Computed Properties

  • Exact Mass: 146.03400

Experimental Properties

  • Boiling Point: 105-110
  • PSA: 0.00000
  • LogP: 2.41230

2,4,6-Trifluorotoluene Security Information

  • Hazard Statement: Flammable
  • Hazardous Material Identification: F

2,4,6-Trifluorotoluene Customs Data

  • HS CODE:2903999090
  • Customs Data:

    China Customs Code:

    2903999090

    Overview:

    2903999090 Other aromatic halogenated derivatives. VAT:17.0% Tax refund rate:9.0% Regulatory conditions:nothing MFN tariff:5.5% general tariff:30.0%

    Declaration elements:

    Product Name, component content, use to

    Summary:

    2903999090 halogenated derivatives of aromatic hydrocarbons VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:5.5% General tariff:30.0%

2,4,6-Trifluorotoluene Pricemore >>

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2,4,6-Trifluorotoluene Production Method

Production Method 1

Reaction Conditions
Reference
Reaction of aromatic compounds with nucleophilic reagents in a liquid ammonia medium. IV. Nucleophilic and protophilic activity of methylate and hydroxyl anions in reactions with polyfluoroaromatic compounds
Shtark, A. A.; Chuikova, T. V.; Shteingarts, V. D., Zhurnal Organicheskoi Khimii, 1984, 20(5), 1055-63

Production Method 2

Reaction Conditions
1.1 Reagents: Tetraethylsilane Catalysts: 7,8,9,10,11,12-Hexabromo-2,3,4,5,6-pentahydro-1-(trimethylsilyl)-1-carbadodecabo… ;  24 h, 160 °C
Reference
Catalytically Generated Meerwein's Salt-Type Oxonium Ions for Friedel-Crafts C(sp2)-H Methylation with Methanol
He, Tao ; Klare, Hendrik F. T. ; Oestreich, Martin, Journal of the American Chemical Society, 2023, 145(6), 3795-3801

Production Method 3

Reaction Conditions
Reference
Preparation of fluorotoluene derivatives
, China, , ,

Production Method 4

Reaction Conditions
1.1 Reagents: Sodium amide Solvents: Ammonia
1.2 Solvents: Ammonia
Reference
Reaction of aromatic compounds with nucleophilic agents in liquid ammonia. IX. Reaction of polyfluorobenzenes with sodium amide
Shtark, A. A.; Chuikova, T. V.; Selivanova, G. A.; Shteingarts, V. D., Zhurnal Organicheskoi Khimii, 1987, 23(12), 2574-80

2,4,6-Trifluorotoluene Raw materials

2,4,6-Trifluorotoluene Preparation Products

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