Basic information Safety Supplier Related

2-AMINO-5-CHLORO-2',6'-DIFLUOROBENZOPHENONE

Basic information Safety Supplier Related

2-AMINO-5-CHLORO-2',6'-DIFLUOROBENZOPHENONE Basic information

Product Name:
2-AMINO-5-CHLORO-2',6'-DIFLUOROBENZOPHENONE
Synonyms:
  • 2-Amino-5-chloro-2',6'-difluorobenzophenone 98%
  • 2-AMINO-5-CHLORO-2',6'-DIFLUOROBENZOPHENONE
  • 2-AMINO-5-CHLORO-PHENYL-(2-6-DIFLUORO-PHENYL)-METHANONE
  • 2-Amino-5-chloro-2',6'-difluorobenzophenone 98+%
  • 6-benzoyl-4-chloro-1,5-difluorocyclohexa-2,4-dien-1-aMine
  • Methanone, (2-amino-5-chlorophenyl)(2,6-difluorophenyl)-
  • 4-chloro-2-(2,6-difluorobenzoyl)aniline
  • 2-Amino-5-chloro-2′,6′-difluoro-benzophenone, CAS 28910-83-0
CAS:
28910-83-0
MF:
C13H8ClF2NO
MW:
267.66
Product Categories:
  • Building Blocks/Intermediates
  • Amines
  • Aromatics
Mol File:
28910-83-0.mol
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2-AMINO-5-CHLORO-2',6'-DIFLUOROBENZOPHENONE Chemical Properties

Melting point:
151-153°C
Boiling point:
435.2±45.0 °C(Predicted)
Density 
1.407±0.06 g/cm3(Predicted)
storage temp. 
Keep in dark place,Inert atmosphere,Room temperature
solubility 
DMSO (Slightly), Methanol (Slightly)
form 
Solid
pka
-1.71±0.10(Predicted)
color 
Yellow
InChI
InChI=1S/C13H8ClF2NO/c14-7-4-5-11(17)8(6-7)13(18)12-9(15)2-1-3-10(12)16/h1-6H,17H2
InChIKey
DUMGVPIXKALANS-UHFFFAOYSA-N
SMILES
C(C1=CC(Cl)=CC=C1N)(C1=C(F)C=CC=C1F)=O
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Safety Information

HS Code 
2922390090
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2-AMINO-5-CHLORO-2',6'-DIFLUOROBENZOPHENONE Usage And Synthesis

Chemical Properties

Yellow Solid

Uses

2-Aminobenzophenone derivative.

Synthesis

869365-92-4

28910-83-0

The general procedure for the synthesis of 2-amino-5-chloro-2,6-difluorobenzophenone using [4-chloro-2-(2,6-difluorobenzyl)phenyl]-carbamic acid-1,1-dimethylethyl ester as a starting material was as follows: the N-Boc-protected aminobenzophenone was dissolved in anhydrous dichloromethane (50 mL), followed by the addition of trifluoroacetic acid (50 mL). The reaction mixture was stirred for 1 h at room temperature and then the solvent was evaporated to dryness by rotary evaporator under vacuum. The resulting residue was dissolved in a mixture of ethyl acetate (100 mL) and saturated aqueous sodium bicarbonate (100 mL). The organic phase was separated and washed with saturated aqueous sodium bicarbonate solution and subsequently dried with anhydrous magnesium sulfate. The dried organic phase was concentrated to dryness by rotary evaporator and the target product 2-amino-5-chloro-2,6-difluorobenzophenone was quantitatively obtained, and mass spectrometry analysis showed m/z = 268 (M + H).

References

[1] Patent: US2005/256102, 2005, A1. Location in patent: Page/Page column 140
[2] Angewandte Chemie - International Edition, 2012, vol. 51, # 27, p. 6598 - 6603

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