2,4-DIFLUOROBENZAMIDE

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CAS:85118-02-1
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CAS:85118-02-1
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CAS:85118-02-1
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CAS:85118-02-1
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Products Intro: Product Name:2,4-difluorobenzamide
CAS:85118-02-1
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2,4-DIFLUOROBENZAMIDE manufacturers

  • 2,4-DIFLUOROBENZAMIDE
  • 2,4-DIFLUOROBENZAMIDE pictures
  • $1.00 / 1kg
  • 2019-07-06
  • CAS:85118-02-1
  • Min. Order: 1kg
  • Purity: 99%
  • Supply Ability: 200kg
2,4-DIFLUOROBENZAMIDE Basic information
Product Name:2,4-DIFLUOROBENZAMIDE
Synonyms:2,4-DIFLUOROBENZAMIDE;DIFLUORO BENZAMIDE;Benzamide, 2,4-difluoro-;2,4-fluorobenzamide;2,4-Difluorobenzamide 99%;2,4-Difluorobenzamide99%
CAS:85118-02-1
MF:C7H5F2NO
MW:157.12
EINECS:285-654-7
Product Categories:Anilines, Amides & Amines;Fluorine Compounds;Amides;Carbonyl Compounds;Organic Building Blocks
Mol File:85118-02-1.mol
2,4-DIFLUOROBENZAMIDE Structure
2,4-DIFLUOROBENZAMIDE Chemical Properties
Melting point 161-165 °C (lit.)
Boiling point 200.4±30.0℃ (760 Torr)
density 1.348±0.06 g/cm3 (20 ºC 760 Torr)
Fp 75.0±24.6℃
storage temp. Sealed in dry,Room Temperature
pka15.19±0.50(Predicted)
form solid
AppearanceWhite to off-white Solid
InChI1S/C7H5F2NO/c8-4-1-2-5(7(10)11)6(9)3-4/h1-3H,(H2,10,11)
InChIKeyKTXFXDMDYZIXSJ-UHFFFAOYSA-N
SMILESNC(=O)c1ccc(F)cc1F
CAS DataBase Reference85118-02-1(CAS DataBase Reference)
Safety Information
Hazard Codes Xi
Risk Statements 36/37/38
Safety Statements 26-36-36/37
WGK Germany 3
HazardClass IRRITANT
HS Code 2924297099
Storage Class11 - Combustible Solids
MSDS Information
ProviderLanguage
SigmaAldrich English
ALFA English
2,4-DIFLUOROBENZAMIDE Usage And Synthesis
Chemical Propertieswhite to light yellow crystal powde
Synthesis
2,4-Difluorobenzoyl chloride

72482-64-5

2,4-DIFLUOROBENZAMIDE

85118-02-1

General procedure for the synthesis of 2,4-difluorobenzamide from 2,4-difluorobenzoyl chloride: in a 250 mL three-necked flask, 150 mL of ammonia was added and cooled down to -10°C. The concentrate of 2,4-difluorobenzoyl chloride was added slowly dropwise, and the reaction was kept incubated for 0.5 h at -10°C, and then brought up to room temperature and continued for 1 h. The reaction was completed by filtration. After completion of the reaction, the product was separated by filtration and the filter cake was dried under vacuum to give 23.8 g of 2,4-difluorobenzamide in 95.5% yield.

References[1] Patent: CN106854165, 2017, A. Location in patent: Paragraph 0102; 0103; 0134; 0135
2,4-DIFLUOROBENZAMIDE Preparation Products And Raw materials
Raw materials2,4-Difluorobenzoyl chloride
Tag:2,4-DIFLUOROBENZAMIDE(85118-02-1) Related Product Information
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