4-AMINO-2,6-DIBROMOPHENOL
4-AMINO-2,6-DIBROMOPHENOL Basic information
- Product Name:
- 4-AMINO-2,6-DIBROMOPHENOL
- Synonyms:
-
- ASISCHEM U70323
- 4-hydroxy-3,5-dibromoaniline
- 4-amino-2,6-dibromo-pheno
- Phenol, 4-amino-2,6-dibromo-
- TIMTEC-BB SBB006577
- 4-AMINO-2,6-DIBROMOPHENOL
- 3,5-DIBROMO-4-HYDROXYANILINE
- 2,6-DIBROMO-4-AMINOPHENOL
- CAS:
- 609-21-2
- MF:
- C6H5Br2NO
- MW:
- 266.92
- EINECS:
- 210-185-1
- Product Categories:
-
- Building Blocks
- C6 to C8
- Phenol&Thiophenol&Mercaptan
- Chemical Synthesis
- Organic Building Blocks
- Oxygen Compounds
- Anilines, Amides & Amines
- Bromine Compounds
- Phenols
- Mol File:
- 609-21-2.mol
4-AMINO-2,6-DIBROMOPHENOL Chemical Properties
- Melting point:
- 195-196 °C(lit.)
- Boiling point:
- 295.6±40.0 °C(Predicted)
- Density
- 2.0444 (rough estimate)
- refractive index
- 1.6400 (estimate)
- storage temp.
- 2-8°C(protect from light)
- pka
- 7.17±0.23(Predicted)
- BRN
- 2803732
- CAS DataBase Reference
- 609-21-2(CAS DataBase Reference)
- EPA Substance Registry System
- Phenol, 4-amino-2,6-dibromo- (609-21-2)
Safety Information
- Hazard Codes
- Xi
- Risk Statements
- 36/37/38
- Safety Statements
- 26-37/39-36
- WGK Germany
- 3
- TSCA
- Yes
- HazardClass
- IRRITANT
- HS Code
- 29222900
MSDS
- Language:English Provider:SigmaAldrich
- Language:English Provider:ACROS
- Language:English Provider:ALFA
4-AMINO-2,6-DIBROMOPHENOL Usage And Synthesis
Chemical Properties
beige to pale brown crystalline powder
Synthesis
The synthesis of 4-amino-2,6-dibromophenol is as follows:4-Nitro-2,6-dibromophenol (2.97g, 10mmol) was dissolved in ethanol (15ml) and water (3ml), and acetic acid (1ml) was added. Then heat and stir to raise the temperature to 80°C, and add iron powder (1.68g, 30mmol) in batches. After the addition is complete, the reaction solution is kept warm for 30 minutes, heating is stopped, filtered while hot, the filtrate is concentrated under reduced pressure, then ethyl acetate and water are added to the concentrated residue to extract, the organic phases are combined and dried, filtered, and the solvent is removed under reduced pressure. The residue was finally separated by column chromatography (ethyl acetate/petroleum ether=1/3) to obtain 4-amino-2,6-dibromophenol (2.52g, 94.4% yield).
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4-AMINO-2,6-DIBROMOPHENOL(609-21-2)Related Product Information
- 2,6-Dibromophenol
- 2-Amino-4,6-dibromophenol
- 4-AMINO-2,6-DIBROMOPHENOL TIN(II)CHLORIDE HYDROCHLORIDE,4-AMINO-2,6-DIBROMOPHENOL CHLOROSTANNATE
- 3,5-DIBROMO-4-HYDROXYPHENYLISOTHIOCYANATE
- 2,6-DIBROMO-3-METHYL-4-NITROPHENOL
- (2,6-dibromo-4-nitrophenoxy)acetic acid
- 3-(2,6-dibromo-4-nitrophenoxy)propanoic acid
- O-BROMOPHENOLINDO-2,6-DIBROMOPHENOL
- 2,6-Dibromo-4-nitrophenol
- Eprotirome
- N-(3,5-DIBROMO-4-HYDROXYPHENYL)(PHENYLCYCLOPENTYL)FORMAMIDE
- 4-AMINO-2,6-DIBROMOPHENOL
- LACMOID
- 4-(3',5'-DIBROMO-4-HYDROXYPHENYL)AMINO-6,7-DIMETHOXYQUINAZOLINE
- 1,3-DIBROMO-2-METHOXY-5-NITROBENZENE