4-Bromo-4'-hydroxybiphenyl
4-Bromo-4'-hydroxybiphenyl Basic information
- Product Name:
- 4-Bromo-4'-hydroxybiphenyl
- Synonyms:
-
- 4'-BROMOBIPHENYL-4-OL
- 4-BROMO-4'-HYDROXYBIPHENYL
- 4-HYDROXY-4'-BROMOBIPHENYL
- 4-(4-BROMPHENYL)-PHENOL
- 4-(4-BROMOPHENYL)PHENOL
- 4- hydroxyl-4’-bromobiphenyl
- 4'-Bromo-(1,1'-biphenyl)-4-ol
- 4-(4-Bromophenyl)phenol,97%
- CAS:
- 29558-77-8
- MF:
- C12H9BrO
- MW:
- 249.1
- EINECS:
- 608-376-3
- Product Categories:
-
- Bromine Compounds
- Phenols
- Bifunctional Compounds (Building Blocks for Liquid Crystals)
- Biphenyls (Building Blocks for Liquid Crystals)
- Building Blocks for Liquid Crystals
- Functional Materials
- Phenols (Building Blocks for Liquid Crystals)
- B
- Stains and Dyes
- Stains&Dyes, A to
- Mol File:
- 29558-77-8.mol
4-Bromo-4'-hydroxybiphenyl Chemical Properties
- Melting point:
- 164-166 °C(lit.)
- Boiling point:
- 355.5±17.0 °C(Predicted)
- Density
- 1.4188 (rough estimate)
- refractive index
- 1.5130 (estimate)
- storage temp.
- Sealed in dry,Room Temperature
- form
- powder to crystal
- pka
- 9.70±0.15(Predicted)
- color
- White to Almost white
- Water Solubility
- Soluble in water (partly), and methanol.
- InChI
- InChI=1S/C12H9BrO/c13-11-5-1-9(2-6-11)10-3-7-12(14)8-4-10/h1-8,14H
- InChIKey
- ARUBXNBYMCVENE-UHFFFAOYSA-N
- SMILES
- C1(C2=CC=C(Br)C=C2)=CC=C(O)C=C1
- CAS DataBase Reference
- 29558-77-8(CAS DataBase Reference)
MSDS
- Language:English Provider:ACROS
- Language:English Provider:SigmaAldrich
- Language:English Provider:ALFA
4-Bromo-4'-hydroxybiphenyl Usage And Synthesis
Chemical Properties
White or cream powder
Uses
A biphenyl starting material. 4?-Bromo-(1,1?-biphenyl)-4-ol is a useful intermediate. Vinylation of 4-bromo-4?-hydroxybiphenyl and ethyl acrylate using Pd (OAc) 2/PPh 3 catalyst was studied. Ethyl 4-(4?-hydroxyphenyl) cinnamate was formed as the vinylation product, while, 4-hydroxybiphenyl and ethyl cinnamate were formed as side products. Preparation of 4-cyano-4'-hydroxybiphenyl This was prepared from 4-bromo-4'-benzenesulphonyloxybiphenyl by first hydrolysing it to 4-bromo-4-hydroxybiphenyl using sodium hydroxide dissolved in a mixture of water and dioxan. The syntheses of the Nanocomposite dendrimers based on cyclic phosphazene cores: Amorphous materials, were accomplished by following a modified literature procedure by reacting phosphonitrilic chloride trimer with 4-bromophenol or 4-bromo-4?-hydroxybiphenyl, respectively, in the presence of K 2 CO 3 in tetrahydrofuran (THF).
4-Bromo-4'-hydroxybiphenylSupplier
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4-Bromo-4'-hydroxybiphenyl(29558-77-8)Related Product Information
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