2,5-Difluorophenylhydrazine hydrochloride
2,5-Difluorophenylhydrazine hydrochloride Basic information
- Product Name:
- 2,5-Difluorophenylhydrazine hydrochloride
- Synonyms:
-
- 2,5-DIFLUOROPHENYLHYDRAZINE HYDROCHLORIDE
- 2,5-DifluorophenylhydrazineHCl
- 2,5-Difluorophenylhydrazine hydrochloride 97%
- 2,5-Difluorophenylhydrazinehydrochloride97%
- 2,5-Difluorphenylhydrazinehydrochloride
- 2,5-Difluorophenylhydrazine HCI
- 1,4-Difluoro-2-hydrazinobenzene hydrochloride
- 2,5-Difluorophenylhy
- CAS:
- 175135-73-6
- MF:
- C6H7ClF2N2
- MW:
- 180.58
- Product Categories:
-
- Aromatic Hydrazides, Hydrazines, Hydrazones and Oximes
- Phenylhydrazine
- Miscellaneous
- Mol File:
- 175135-73-6.mol
2,5-Difluorophenylhydrazine hydrochloride Chemical Properties
- Melting point:
- 210°C
- storage temp.
- Sealed in dry,Room Temperature
- Appearance
- Light brown to yellow Solid
- BRN
- 8640307
- CAS DataBase Reference
- 175135-73-6(CAS DataBase Reference)
Safety Information
- Hazard Codes
- Xi
- Risk Statements
- 20/21/22-36/37/38-22
- Safety Statements
- 22-36/37/39-36/37-26
- RIDADR
- 2811
- Hazard Note
- Irritant
- PackingGroup
- III
- HS Code
- 29280000
MSDS
- Language:English Provider:2,5-Difluorophenylhydrazine hydrochloride
- Language:English Provider:ALFA
2,5-Difluorophenylhydrazine hydrochloride Usage And Synthesis
Uses
2,5-Difluorophenylhydrazine, HCl
Synthesis
Using 2,5-difluoroaniline as raw material, in 3 times the amount of concentrated hydrochloric acid, glacial acetic acid as a co-solvent, and adding 3% of the mass of raw material PEG-400 as a phase-transfer catalyst, the diazotization reaction was carried out at -5 ?? 0 ?? for 1 h with 1.05 times the amount of molar sodium nitrite (prepared as an aqueous solution). 1.05 times the molar amount of sodium nitrite (prepared as an aqueous solution) -5 ~ 0 ?? under the condition of diazotization reaction for 1 h; sodium bisulfite as a reducing agent, diazotization solution 75 ?? reduction reaction 1h, the resulting reduction products were used as the phase transfer catalyst, and the phase transfer catalyst was used as the phase transfer catalyst. 1h, the obtained reduction product was acid precipitated by concentrated hydrochloric acid at 85 ?? for 2 h, . 2,5-difluorophenylhydrazine hydrochloride was prepared; finally, 2,5-difluorophenylhydrazine hydrochloride could be obtained by alkaline hydrolysis of 2,5-difluorophenylhydrazine hydrochloride with sodium hydroxide, the content ??96% (HPLC), the yield was ??74% (with 2,5-difluorophenylhydrazine hydrochloride). ??74% (as 2,5-difluorophenylhydrazine).
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