10-366615 - 2-1-adamantylaminoethanol | 3716-66-3

<p>Applications 1-Adamantanemethanol is used as a reagent in the synthesis of adamantane and noradamantane based histone deacetylase (HDAC) inhibitors for the treatment of cancer. It is also used as a reagent in the synthesis of (1-adamantyl)methyl glycidyl ether, a versatile building block for living polymerization.<br>References Gopalan, B., et al.: Bioorg. Med. Chem. Lett., 23, 2532 (2013); Suzuki, T., et al.: J. Med. Chem., 55, 9562 (2012); Moers, C., et al.: Macromol. Rapid Comm., 35, 1075 (2014)<br></p>

<p>1-Adamantanemethanol was used in the synthesis of axially disubstituted silicon(IV) phthalocyanines. It is used as a reagent in the synthesis of adamantane and noradamantane based histone deacetylase (HDAC) inhibitors for the treatment of cancer. It is also used as a reagent in the synthesis of (1-a</p>

<p>1-(Hydroxymethyl)adamantane</p>

<p>3-Hydroxy-1-adamantanemethanol</p>

<p>Adamantanemethanol is a molecule used in the process of translation. It is structurally analyzed by trifluoromethanesulfonic acid, which is a cavity. The pharmacokinetic properties of adamantanemethanol are determined by its acyl chain. Adamantanemethanol has been studied in clinical trials, and the minimal inhibitory concentration for this drug is determined by chloride. This molecule also forms hydrogen bonds with hydroxyl groups and functional groups. Adamantanemethanol has been shown to be an effective antimicrobial agent against bacterial replication in cell culture and has optical properties that can be used to identify it.</p>

<p>3-(Hydroxymethyl)-1-adamantol is an ester that is formed by the reaction of adapalene with ethyl chloroformate. This product is produced as a byproduct of the synthesis of adapalene, which is a topical acne medication. 3-(Hydroxymethyl)-1-adamantol can be recycled and used to produce other compounds through ion-exchange chromatography, filtration, or hydrogenation. This compound interacts with sodium borohydride to produce 1-adamantanol, which has been shown to have anti-inflammatory properties in vitro. The yield for this reaction can be increased when triethylamine is added.</p>