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2,5-Dichlorofluorobenzene

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2,5-Dichlorofluorobenzene manufacturers

2,5-Dichlorofluorobenzene Basic information
Product Name:2,5-Dichlorofluorobenzene
Synonyms:1,4-Dichloro-2-fluorobenzene, 99+%;2,5-dichloro-1-fluorobenzene;2,5-Dichlorofluorobenzene 98%;2,5-Dichlorofluorobenzene98%;1,4-Dichloro-2-fluorobenzene, 99+% 5GR;Benzene,1,4-dichloro-2-fluoro-;2,5-dichloro-fluorophenyl;2-Oxopentanedioic acid - L-ornithine (1:1)
CAS:348-59-4
MF:C6H3Cl2F
MW:164.99
EINECS:
Product Categories:Chlorine Compounds;Fluorine Compounds;Fluorine series;Other fluorin-contained compounds
Mol File:348-59-4.mol
2,5-Dichlorofluorobenzene Structure
2,5-Dichlorofluorobenzene Chemical Properties
Melting point 4 °C
Boiling point 168 °C
density 1.383
refractive index 1.5235-1.5255
Fp 65 °C
storage temp. Sealed in dry,Room Temperature
solubility Difficult to mix.
form clear liquid
Specific Gravity1.383
color Colorless to Light yellow to Light orange
BRN 2355590
CAS DataBase Reference348-59-4(CAS DataBase Reference)
Safety Information
Hazard Codes Xi
Risk Statements 36/37/38
Safety Statements 37/39-26
RIDADR 1992
Hazard Note Irritant
PackingGroup III
HS Code 29036990
MSDS Information
ProviderLanguage
ACROS English
ALFA English
2,5-Dichlorofluorobenzene Usage And Synthesis
Chemical PropertiesCLEAR COLORLESS LIQUID
Uses1,4-Dichloro-2-fluorobenzene is used as organic synthesis intermediates
Synthesis
2,5-Dichloroaniline

95-82-9

2,5-DICHLOROFLUOROBENZENE

348-59-4

General procedure for the synthesis of 2,5-dichlorofluorobenzene from 2,5-dichloroaniline: 1. Continuous diazotization step: material A (50 mL aqueous solution containing 2,5-dichloroaniline (100 mmol), fluoboric acid (120 mmol) and hydrochloric acid (180 mmol)) was pumped through a T-fitting into a reaction tube at a flow rate of 4 mL/min at 25°C with material B (50 mL aqueous solution containing sodium nitrite (105 mmol)), the mixture flowed through the outlet and collected in a cooling vessel. Vigorous stirring was maintained. The slurry was cooled to -5 °C and then diafiltrated. The solid was washed with methanol and subsequently dried under vacuum to give 2,5-dichlorobenzenediazonium tetrafluoroborate. 2. Continuous fluorination step: a slurry of 2,5-dichlorobenzenediazonium tetrafluoroborate prepared above in 300 mL of co-solvent was introduced continuously into a reaction tube at a flow rate of 4 mL/min. The mixture was kept at the set temperature for 1 min and subsequently cooled in the tandem tube. The collected liquid was washed with aqueous NaOH and water to give an almost colorless liquid of 2,5-dichlorofluorobenzene.

References[1] Tetrahedron Letters, 2013, vol. 54, # 10, p. 1261 - 1263
[2] Journal of the American Chemical Society, 1959, vol. 81, p. 94,95, 97
[3] Journal of the American Chemical Society, 1953, vol. 75, p. 4590
[4] Acta Chimica Academiae Scientiarum Hungaricae, 1957, vol. 10, p. 227,229
2,5-Dichlorofluorobenzene Preparation Products And Raw materials
Raw materials2,5-Dichloroaniline-->Fluoroboric acid-->Sodium nitrite-->Hydrochloric acid
Tag:2,5-Dichlorofluorobenzene(348-59-4) Related Product Information
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