187054

4-Bromobenzyl alcohol

99%

• Sinónimos: (4-Bromophenyl)methanol, (p-Bromophenyl)methanol, 1-(p-Bromophenyl)methanol, 1-Bromo-4-(hydroxymethyl)benzene, 4-Hydroxymethyl-1-bromobenzene, p-Bromobenzyl alcohol
• Fórmula lineal: BrC₆H₄CH₂OH
• Número de CAS: 873-75-6
• Peso molecular: 187.03
• Beilstein/REAXYS Number: 1931620
• EC Number: 212-851-7
• MDL number: MFCD00004650
• UNSPSC Code: 12352100
• PubChem Substance ID: 24851248
• NACRES: NA.22

Propiedades

• Quality Level: 100
• assay: 99%
• form: solid
• mp: 75-77 °C (lit.)
• solubility: dioxane: soluble 1 g/10 mL, clear to faintly turbid, colorless to faintly yellow
• functional group: bromo; hydroxyl
• SMILES string: OCc1ccc(Br)cc1
• InChI: 1S/C7H7BrO/c8-7-3-1-6(5-9)2-4-7/h1-4,9H,5H2
• InChI key: VEDDBHYQWFOITD-UHFFFAOYSA-N
• Gene Information: human ... ALOX12(239) , ALOX15(246)

Descripción

General description

4-Bromobenzyl alcohol undergoes three-component reaction with acetylferrocene and arylboronic acid to give ferrocenyl ketones containing biaryls. It undergoes oxidation reaction in the presence of polyvinylpolypyrrolidone-supported hydrogen peroxide, silica sulfuric acid and ammonium bromide to yield 4-bromobenzaldehyde. It undergoes efficient trimethylsilylation reaction with 1,1,1,3,3,3-hexamethyldisilazane in the presence of catalytic amount of aspartic acid in acetonitrile.

Application

4-Bromobenzyl alcohol was used in the synthesis of:

• hydroxyl end functionalized, substituted polyfluorene
• amphiphilic, symmetric rod-coil, triblock copolymer of poly(9,9-didodecylfluorene-2,7-diyl) and poly(hydroxyl ethyl methacrylate)

Información de seguridad

• hcodes: H412
• pcodes: P273 - P501
• Hazard Classifications: Aquatic Chronic 3
• Storage Class: 13 - Non Combustible Solids
• wgk_germany: WGK 3
• flash_point_f: Not applicable
• flash_point_c: Not applicable
• ppe: Eyeshields, Gloves, type N95 (US)