1,3-Dichloro-2-fluorobenzene
1,3-Dichloro-2-fluorobenzene Basic information
- Product Name:
- 1,3-Dichloro-2-fluorobenzene
- Synonyms:
-
- 1,3-Dichloro-2-fluor
- 1,3-Dicchloro-2-fluorobenzene
- 1,3-DICHLORO-2-FLUOROBENZENE
- 2,6-DICHLOROFLUOROBENZENE
- Benzene,1,3-dichloro-2-fluoro-
- 2,6-DichloroFluorobenzene99%
- 2,6-Dichloro Fluorobenzene 99%
- 1,3-Dichloro-2-fluorobenzene, 98+%
- CAS:
- 2268-05-5
- MF:
- C6H3Cl2F
- MW:
- 164.99
- EINECS:
- 607-128-1
- Product Categories:
-
- Halogenated Hydrocarbons
- Aryl
- C6
- Mol File:
- 2268-05-5.mol
1,3-Dichloro-2-fluorobenzene Chemical Properties
- Melting point:
- 37-40 °C(lit.)
- Boiling point:
- 168-169 °C(lit.)
- Density
- 1.3967 (estimate)
- Flash point:
- 140 °F
- storage temp.
- Sealed in dry,Room Temperature
- form
- powder to crystal
- color
- White to Light yellow to Light orange
- BRN
- 1862513
- InChI
- InChI=1S/C6H3Cl2F/c7-4-2-1-3-5(8)6(4)9/h1-3H
- InChIKey
- JORVCRLRRRRLFI-UHFFFAOYSA-N
- SMILES
- C1(Cl)=CC=CC(Cl)=C1F
- CAS DataBase Reference
- 2268-05-5(CAS DataBase Reference)
- NIST Chemistry Reference
- 1,3-Dichloro-2-fluorobenzene(2268-05-5)
Safety Information
- Hazard Codes
- Xi
- Risk Statements
- 36/37/38
- Safety Statements
- 26-36-37/39
- RIDADR
- UN 1325 4.1/PG 2
- WGK Germany
- 2
- Hazard Note
- Irritant
- HazardClass
- 4.1
- PackingGroup
- III
- HS Code
- 2903998090
MSDS
- Language:English Provider:SigmaAldrich
- Language:English Provider:ACROS
- Language:English Provider:ALFA
1,3-Dichloro-2-fluorobenzene Usage And Synthesis
Chemical Properties
slightly beige transparent crystals
Synthesis
2106-49-2
2268-05-5
The general procedure for the synthesis of 2,6-dichlorofluorobenzene from 3-chloro-2-fluoronitrobenzene is as follows: In a 250 ml four-necked flask, 240 g (1.368 mol) of 3-chloro-2-fluoronitrobenzene was added and the temperature was raised to 180°C. Dry chlorine gas was passed through the flask, and the temperature of the reaction was controlled to be between 180 and 190°C. The reaction was carried out by distillation. Distillation was carried out during the reaction for 8 to 10 hours. The fractions are collected and sequentially washed with water and alkali to a weak base. The organic phase was separated and subjected to vacuum distillation, resulting in 210 g of 2,6-dichlorofluorobenzene with 99.7% purity and 93% yield.
References
[1] Patent: CN102249881, 2016, B. Location in patent: Paragraph 0015; 0050-0051
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