4-Benzyloxy-1-bromobenzene

CAS : 6793-92-6

Ref. 3D-FB18438

Informations sur le produit

• Nom: 4-Benzyloxy-1-bromobenzene
• Synonymes: Benzyl p-bromophenyl ether1-Bromo-4-(benzyloxy)benzene1-Bromo-4-(phenylmethoxy)benzene, 1-Benzyloxy-4-bromobenzene, 1-Bromo-4-(benzyloxy)benzene, 1-Bromo-4-(phenylmethoxy)benzene, 1-Bromo-4-[(phenylmethyl)oxy]benzene, 1-Bromo-4-benzyloxybenzene, 4-(Benzyloxy)bromobenzene, 4-Benzyloxybromobenzene, 4-Bromophenyl benzyl ether, 5-(Tert-Butyldimethylsilyl)-1-Methyl-1H, Benzene, 1-bromo-4-(phenylmethoxy)-, Benzyl 4-bromophenyl ether, Benzyl p-bromophenyl ether, Ether, benzyl p-bromophenyl, p-(Benzyloxy)bromobenzene, p-(Benzyloxy)phenyl bromide, p-Bromophenyl benzyl ether
• CAS: 6793-92-6

Description

4-Benzyloxy-1-bromobenzene is a halide that can be synthesized by reacting 4-hydroxybenzaldehyde with 1-bromoethane in the presence of copper(II) acetate. This reaction is catalyzed by copper(II) acetate and occurs at room temperature. The product has an enantiomeric purity of 99% and is a scalable synthesis, which makes it ideal for commercial production. It has been shown to bind to the CB1 receptor, which may lead to therapeutic applications. 4-Benzyloxy-1-bromobenzene has also been shown to have estrogenic activity and may be used as a synthetic precursor to drugs that are metabolized by CYP3A4.

• Marque: Biosynth

Propriétés chimiques

• Masse moléculaire: 263.13 g/mol
• Formule: C₁₃H₁₁BrO
• Degré de pureté: Min. 95%
• Couleur/Forme: Powder
• InChI: InChI=1S/C13H11BrO/c14-12-6-8-13(9-7-12)15-10-11-4-2-1-3-5-11/h1-9H,10H2
• Code InChI: InChIKey=OUQSGILAXUXMGI-UHFFFAOYSA-N
• SMILES: Brc1ccc(OCc2ccccc2)cc1