2,4-Difluorobromobenzene
1-Bromo-2,4-difluorobenzene
CAS: 348-57-2
Molecular Formula: C6H3BrF2
2,4-Difluorobromobenzene - Names and Identifiers
| Name | 1-Bromo-2,4-difluorobenzene |
| Synonyms | 2,4-Difluoro 2,4-Difluorobromobenzene 2,4-DIFLUOROBROMOBENZENE Bromo-2,4-difluorobenzene 1-Bromo-2,4-difluorobenzene 2,4-Difluoro-1-bromobenzene 1-BROMO-2,4-DIFLUOROBENZENE 1,4-dichloro-2-fluorobenzene Benzene, 1-bromo-2,4-difluoro- |
| CAS | 348-57-2 |
| EINECS | 206-479-4 |
| InChI | InChI=1/C6H3Cl2F/c7-4-1-2-5(8)6(9)3-4/h1-3H |
| InChIKey | MGHBDQZXPCTTIH-UHFFFAOYSA-N |
2,4-Difluorobromobenzene - Physico-chemical Properties
| Molecular Formula | C6H3BrF2 |
| Molar Mass | 192.99 |
| Density | 1.708 g/mL at 25 °C (lit.) |
| Melting Point | -4 °C (lit.) |
| Boling Point | 145-146 °C (lit.) |
| Flash Point | 125°F |
| Water Solubility | INSOLUBLE |
| Vapor Presure | 1.94mmHg at 25°C |
| Appearance | Liquid |
| Specific Gravity | 1.708 |
| Color | Clear colorless to brown |
| BRN | 1680892 |
| PH | 5.02 at 24℃ and 10g/L |
| Storage Condition | Sealed in dry,2-8°C |
| Refractive Index | n20/D 1.505(lit.) |
| Physical and Chemical Properties | density 1.708 melting point -4°C boiling point 145°C refractive index 1.504-1.506 flash point 51°C water-soluble INSOLUBLE |
| Use | For pharmaceutical or liquid crystal material intermediates |
2,4-Difluorobromobenzene - Risk and Safety
| Risk Codes | R10 - Flammable R36/37/38 - Irritating to eyes, respiratory system and skin. |
| Safety Description | S16 - Keep away from sources of ignition. S26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. S36/37/39 - Wear suitable protective clothing, gloves and eye/face protection. S37/39 - Wear suitable gloves and eye/face protection S36 - Wear suitable protective clothing. |
| UN IDs | UN 1993 3/PG 3 |
| WGK Germany | 3 |
| HS Code | 29036990 |
| Hazard Note | Flammable |
| Hazard Class | 3 |
| Packing Group | III |
2,4-Difluorobromobenzene - Nature
Open Data Verified Data
colorless transparent liquid. Melting Point -4 ℃, boiling point 145~146 ℃, relative density 1.708, refractive index 1. 505. Miscible with benzene.
Last Update：2024-01-02 23:10:35
2,4-Difluorobromobenzene - Preparation Method
Open Data Verified Data
derived from the bromination of M-difluorobenzene. Mixing M-difluorobenzene with carbon tetrachloride and iron powder, stirring and heating to about 45 ° C., slowly adding a solution consisting of bromine and carbon tetrachloride, and stirring was continued for 30min after dropping until no white smoke was generated. After cooling, 20% sodium bisulfite solution was added and stirred until colorless. The organic layer was separated, washed with 10% sodium hydroxide and washed with water until neutral. Dry overnight with anhydrous sodium sulfate. The product was obtained by carrying out atmospheric distillation and collecting the fraction at 144-148 ° C. In a yield of 83%.
Last Update：2022-01-01 10:40:36
2,4-Difluorobromobenzene - Use
Open Data Verified Data
for the synthesis of broad-spectrum low toxicity deep antifungal drugs such as fluconazole.
Last Update：2022-01-01 10:40:35
2,4-Difluorobromobenzene - Safety
Open Data Verified Data
packed in 50kg iron plastic barrel.
Last Update：2022-01-01 10:40:36
2,4-Difluorobromobenzene - Reference Information
| NIST chemical information | Information provided by: webbook.nist.gov (external link) |
| uses | intermediates for the synthesis of broad-spectrum low-toxic deep antifungal drugs such as fluconazole (fluconazole). Used as an intermediate in medicine or liquid crystal materials |
| production method | is obtained by bromination of m-difluorobenzene. Mix m-difluorobenzene with carbon tetrachloride and iron powder, stir and heat to about 45 ℃, slowly add a solution composed of bromine and carbon tetrachloride, and continue to stir for 30min after dripping until colorless smoke is produced. Cool, add 20% sodium bisulfite solution and stir until colorless. The organic layer is separated, washed with 10% sodium hydroxide solution, and washed with water until neutral. Dry overnight with anhydrous sodium sulfate. Carry out atmospheric distillation and collect the fraction at 144-148 ℃ to obtain this product with a yield of 83%. |
Last Update：2024-04-09 21:11:58
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CAS: 348-57-2
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