1155843-79-0 | 2-Hydroxy-2-azaadamantane

Packsize	Purity	Availability	Price	Discounted Price
200mg	98%	in stock	$107.00	$75.00
5g	98%	in stock	$1,161.00	$813.00

Description

• Catalog Number: AE16000
• Chemical Name: 2-Hydroxy-2-azaadamantane
• CAS Number: 1155843-79-0
• Molecular Formula: C9H15NO
• Molecular Weight: 153.2215
• MDL Number: MFCD27976826
• SMILES: ON1C2CC3CC1CC(C2)C3

Upstream Synthesis Route

2-Hydroxy-2-azaadamantane, commonly known as hydroxyaziridine, is a versatile compound widely used in chemical synthesis due to its unique structure and reactivity. This compound plays a crucial role in various organic reactions and serves as a valuable building block in the formation of complex molecules.In the realm of chemical synthesis, 2-Hydroxy-2-azaadamantane acts as a key intermediate in the preparation of a wide range of functionalized compounds. Its hydroxy group provides a site for further derivatization, allowing chemists to introduce diverse functional groups and modify the compound according to specific synthetic needs. Additionally, the azaadamantane framework brings rigidity and steric effects to the molecule, influencing its behavior in subsequent reactions.One of the significant applications of 2-Hydroxy-2-azaadamantane lies in its use as a chiral auxiliary in asymmetric synthesis. By incorporating this compound into reactions, chemists can induce chirality and control the stereochemistry of the products. This feature is particularly valuable in the production of enantiomerically pure compounds, which are essential in pharmaceutical and fine chemical industries.Furthermore, 2-Hydroxy-2-azaadamantane is employed as a protecting group in organic synthesis to shield sensitive functional groups during transformations. This temporary protection strategy ensures selective reactions and minimizes unwanted side products, ultimately enhancing the efficiency of the synthetic process.Overall, the versatile nature of 2-Hydroxy-2-azaadamantane in chemical synthesis makes it a valuable tool for organic chemists striving to access complex molecular architectures with precise control over stereochemistry and functional group manipulation.