2-(1-Adamantyl)-4-bromoanisole

CAS: 104224-63-7

Ref. 3D-FA17218

Produktinformation

• Name: 2-(1-Adamantyl)-4-bromoanisole
• Synonyme: 1-(5-Bromo-2-methoxyphenyl)-tricyclo[3.3.1.13,7]decane, 1-(5-Bromo-2-Methosyphenyl)-Tricyclo[3.3.1.13.7]Decane, 1-(5-Bromo-2-Methoxyphenyl)-Tricyclo[3,3,1,13,7]Decane, 1-(5-Bromo-2-Methoxyphenyl)-Tricyclo[3.3.1.13,7]Decane, 1-(5-Bromo-2-Methoxyphenyl)-Trycyclo[3.3.1.13,7]Decane, 1-(5-Bromo-2-Methoxyphenyl)Tricyclo[3.3.1.1~3,7~]Decane, 1-(5-Bromo-2-Methoxyphenyl)Trycyclo[3,3,1,13,7]Decane, 1-(5-Bromo-2-methoxy-phenyl)adamantane, 1-(5-Bromo-2-methoxyphenyl)adamantane, 1-(5-Bromo-2-methoxyphenyl)tricyclo[3.3.1.1^3,7]decane, 1-Methoxy-2-(1-adamantyl)-4-bromobenzene, 2-(1-Adamantyl)-4-Bromo Anisole, 2-(1-Adamantyl)-4-bromomethoxybenzene, 2-(Adamantan-1-yl)-4-bromoanisole, 2-(Adamantan-1-yl)-4-bromo-1-methoxybenzene, 2-Adamantyl-4-bromoanisole, 4-Bromo-2-(1-adamantyl)anisole, Adapalene-2-(1-Adamantyl)-4-bromo-anisole, Tricyclo[3.3.1.13,7]Decane, 1-(5-Bromo-2-Methoxyphenyl)-, Tricyclo[3.3.1.1^3,7]decane, 1-(5-bromo-2-methoxyphenyl)-

Beschreibung

2-(1-Adamantyl)-4-bromoanisole is a molecule that is used as a synthetic intermediate for the preparation of adapalene, which is an acne medication. This molecule has been shown to have dimethylsulfate, ethylene, and grignard reagent properties. 2-(1-Adamantyl)-4-bromoanisole is synthesized from 1-adamantanol and dihedral methylating agents such as methyl iodide or methyl bromide. The localization of this molecule in the body can be determined using centroid analysis by mass spectrometry. 2-(1-Adamantyl)-4-bromoanisole undergoes basic hydrolysis to form bromophenols when exposed to water or alkali metals such as magnesium.

• Marke: Biosynth

Chemische Eigenschaften

• Molekulargewicht: 321.25 g/mol
• Formel: C₁₇H₂₁BrO
• Reinheit: Min. 98 Area-%
• Farbe/Form: Powder
• InChl: InChI=1S/C17H21BrO/c1-19-16-3-2-14(18)7-15(16)17-8-11-4-12(9-17)6-13(5-11)10-17/h2-3,7,11-13H,4-6,8-10H2,1H3
• InChI Key: InChIKey=QQAMHHZQONQBFZ-UHFFFAOYSA-N
• SMILES: COc1ccc(Br)cc1C12CC3CC(CC(C3)C1)C2