2-FLUORO-6-NITROBENZYL BROMIDE
2-FLUORO-6-NITROBENZYL BROMIDE Basic information
- Product Name:
- 2-FLUORO-6-NITROBENZYL BROMIDE
- Synonyms:
-
- 2-FLUORO-6-NITROBENZYL BROMIDE
- 2-Bromomethyl-1-fluoro-3-nitrobenzene
- Benzene, 2-(bromomethyl)-1-fluoro-3-nitro-
- 2-Fluoro-6-nitrobenzyl bromide 98%
- 2-Fluoro-6-nitrobenzylbromide98%
- 2-(Bromomethyl)-1-fluoro-3-nitrobenzene, alpha-Bromo-2-fluoro-6-nitrotoluene
- 2-FLUORO-6-NITROBENZYL BROMIDE ISO 9001:2015 REACH
- 2-fluoro-6-nitrobenzyl bromide2-fluoro-6-nitrobenzyl bromide
- CAS:
- 1958-93-6
- MF:
- C7H5BrFNO2
- MW:
- 234.02
- EINECS:
- 217-801-8
- Product Categories:
-
- API intermediates
- Mol File:
- 1958-93-6.mol
2-FLUORO-6-NITROBENZYL BROMIDE Chemical Properties
- Melting point:
- 53-54°C
- Boiling point:
- 275.5±25.0 °C(Predicted)
- Density
- 1.733±0.06 g/cm3(Predicted)
- storage temp.
- under inert gas (nitrogen or Argon) at 2-8°C
- form
- crystalline powder
- color
- Yellow
- Water Solubility
- Insoluble in water.
- Sensitive
- Lachrymatory
- BRN
- 2503670
- CAS DataBase Reference
- 1958-93-6(CAS DataBase Reference)
Safety Information
- Hazard Codes
- C
- Risk Statements
- 36/37/38
- Safety Statements
- 26-36/37/39-45
- RIDADR
- 3261
- Hazard Note
- Corrosive/Lachrymatory
- HazardClass
- 8
- PackingGroup
- II
- HS Code
- 2904990090
MSDS
- Language:English Provider:ALFA
2-FLUORO-6-NITROBENZYL BROMIDE Usage And Synthesis
Uses
Nitobenzyl ester based nonionic PAGs (NIPAG 2) NIPAG 2 was prepared from 2-fluoro-6-nitrobenzyl bromide with silver sulfonate.
Synthesis
Add 1/3 kettle capacity of carbon tetrachloride solvent and measured azodiisobutyronitrile, 48% hydrogen bromide to the reaction kettle, stirring and heated with steam; heated to about 75 ??, at the same time, drop-addition of measured o-nitrotoluene and 30% hydrogen peroxide, to keep the temperature does not drop to maintain reflux, drop-addition time of about 3-4 hours; drop-addition is completed, continue to hold the reflux reaction for 1-2 hours, turn off the steam, reduce the temperature to Room temperature, take samples to analyze the content of o-nitrobenzyl bromide: liquid separation, the organic layer is washed three times with 20% NaHSO3 aqueous solution and water, and then distilled at atmospheric pressure to remove the carbon tetrachloride solvent; petroleum ether is used for recrystallization of the reaction solution, and then centrifuged the crystals, and cold petroleum ether is used for rinsing, and then the solid product of o-nitrobenzyl bromide is obtained as white color.
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2-FLUORO-6-NITROBENZYL BROMIDE(1958-93-6)Related Product Information
- α-Bromo-2,3,4,5,6-pentafluorotoluene
- 4-Fluorobenzyl bromide
- 1-Fluoro-3-nitrobenzene
- 2-FLUORO-4-NITROBENZYL BROMIDE
- 3-FLUORO-4-NITROBENZYL BROMIDE
- 4-FLUORO-3-NITROBENZYL BROMIDE
- 4-FLUORO-2-NITROBENZYL BROMIDE
- 2-FLUORO-6-NITROBENZYL BROMIDE
- 2-Fluoro-6-nitrotoluene
- 2-Nitrobenzyl bromide
- 2-Fluorobenzyl bromide
- 2-(bromomethyl)-Benzenamine
- 3-Fluoro-2-methylaniline