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1,2-DICHLORO-4-FLUORO-5-NITROBENZENE

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1,2-DICHLORO-4-FLUORO-5-NITROBENZENE Basic information

Product Name:
1,2-DICHLORO-4-FLUORO-5-NITROBENZENE
Synonyms:
  • 1,2-DICHLORO-4-FLUORO-5-NITROBENZENE
  • BUTTPARK 89\07-58
  • 4,5-Dichloro-2-fluoronitrobenzene
  • 1,2-DICHLORO-4-FLUORO-5-NITROBENZENE, 95 %
  • 1,2-DICHLORO-4-FLUORO-5-NITROBENZENE 95%
  • 4,5-Dichloro-2-fluoronitrobenzene 95%
  • 4,5-Dichloro-2-fluoronitrobenzene95%
  • 3,4-Dichloro-2-fluoro-1-nitrobenzene
CAS:
2339-78-8
MF:
C6H2Cl2FNO2
MW:
209.99
Product Categories:
  • Aromatic Halides (substituted)
  • Nitro Compounds
  • Nitrogen Compounds
  • Organic Building Blocks
Mol File:
2339-78-8.mol
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1,2-DICHLORO-4-FLUORO-5-NITROBENZENE Chemical Properties

Melting point:
17 °C (lit.)
Boiling point:
247 °C (lit.)
Density 
1.596 g/mL at 25 °C (lit.)
refractive index 
n20/D 1.575(lit.)
Flash point:
>230 °F
storage temp. 
Sealed in dry,Room Temperature
form 
Low Melting Solid
color 
Pale yellow
InChI
1S/C6H2Cl2FNO2/c7-3-1-5(9)6(10(11)12)2-4(3)8/h1-2H
InChIKey
FXOCDIKCKFOUDE-UHFFFAOYSA-N
SMILES
[O-][N+](=O)c1cc(Cl)c(Cl)cc1F
CAS DataBase Reference
2339-78-8(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xn,Xi
Risk Statements 
20/21/22-36/37/38
Safety Statements 
26-37/39
WGK Germany 
3
Hazard Note 
Irritant
HS Code 
2904990090
Storage Class
10 - Combustible liquids
Hazard Classifications
Acute Tox. 4 Dermal
Acute Tox. 4 Inhalation
Acute Tox. 4 Oral
Eye Irrit. 2
Skin Irrit. 2
STOT SE 3

MSDS

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1,2-DICHLORO-4-FLUORO-5-NITROBENZENE Usage And Synthesis

Chemical Properties

Off-White powder

Uses

1,2-Dichloro-4-fluoro-5-nitrobenzene may be used in the combinatorial solid-phase synthesis of bis-heterocyclic compounds. It was employed as solute to investigate the possibility of selective excitation in coupled multispin systems.

General Description

Proton-detected local field (PDLF) spectra of 1,2-dichloro-4-fluoro-5-nitrobenzene in nematic solvents has been studied.

Synthesis

Acetylation and chlorination in one pot: add 22.2 g of freshly evaporated p-fluoroaniline and 60 mL of glacial acetic acid into the reaction vessel, raise the temperature to 30 ??, and add 20.4 g of acetic anhydride drop by drop under stirring. After the acetic anhydride was added, the reaction was heated to 60-70 ?? and kept warm until the end. Slightly reduce the temperature to 40 ??, slowly introduce Cl2, maintain the reaction temperature at 40 ~ 50 ??, hold the reaction for 12 h, the end of the reaction. The product was poured into 500 mL of ice water, the solid was precipitated, filtered, and the mother liquor was neutralized with Na2CO3 and then filtered to obtain the crude product. Then recrystallized from 60% aqueous ethanol, obtained white needle solid 2-chloro-4-fluoroacetanilide 29.8 g, yield 79.1%.

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