187054

4-Brombenzylalkohol

99%

• Synonym(e): (4-Bromophenyl)methanol, (p-Bromophenyl)methanol, 1-(p-Bromophenyl)methanol, 1-Bromo-4-(hydroxymethyl)benzene, 4-Hydroxymethyl-1-bromobenzene, p-Bromobenzyl alcohol
• Lineare Formel: BrC₆H₄CH₂OH
• CAS-Nummer: 873-75-6
• Molekulargewicht: 187.03
• Beilstein: 1931620
• EG-Nummer: 212-851-7
• MDL-Nummer: MFCD00004650
• UNSPSC-Code: 12352100
• PubChem Substanz-ID: 24851248
• NACRES: NA.22

Eigenschaften

• Qualitätsniveau: 100
• Assay: 99%
• Form: solid
• mp (Schmelzpunkt): 75-77 °C (lit.)
• Löslichkeit: dioxane: soluble 1 g/10 mL, clear to faintly turbid, colorless to faintly yellow
• Funktionelle Gruppe: bromo; hydroxyl
• SMILES String: OCc1ccc(Br)cc1
• InChI: 1S/C7H7BrO/c8-7-3-1-6(5-9)2-4-7/h1-4,9H,5H2
• InChIKey: VEDDBHYQWFOITD-UHFFFAOYSA-N
• Angaben zum Gen: human ... ALOX12(239) , ALOX15(246)

Beschreibung

Allgemeine Beschreibung

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.

Anwendung

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)

Sicherheitshinweise

• H-Sätze: H412
• P-Sätze: P273 - P501
• Gefahreneinstufungen: Aquatic Chronic 3
• Lagerklassenschlüssel: 13 - Non Combustible Solids
• WGK: WGK 3
• Flammpunkt (°F): Not applicable
• Flammpunkt (°C): Not applicable
• Persönliche Schutzausrüstung: Eyeshields, Gloves, type N95 (US)