702-79-4 | 1,3-Dimethyladamantane

Packsize	Purity	Availability	Price	Discounted Price
1g	98%	in stock	$11.00	$8.00
5g	98%	in stock	$13.00	$9.00
10g	98%	in stock	$17.00	$12.00
25g	98%	in stock	$32.00	$22.00

Description

• Catalog Number: AB43147
• Chemical Name: 1,3-Dimethyladamantane
• CAS Number: 702-79-4
• Molecular Formula: C12H20
• Molecular Weight: 164.2872
• MDL Number: MFCD00074755
• SMILES: CC12CC3CC(C1)CC(C2)(C3)C

Computed Properties

• Complexity: 182
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 12
• XLogP3: 4.6

Upstream Synthesis Route

1,3-Dimethyladamantane, also known as rimantadine, is a versatile compound widely used in chemical synthesis. Its unique molecular structure and properties make it an excellent building block in the production of various pharmaceuticals, agrochemicals, and specialty chemicals.One of the key applications of 1,3-Dimethyladamantane in chemical synthesis is its utility as a chiral auxiliary in asymmetric synthesis. Its rigid and symmetric framework allows for precise control over stereochemistry during the formation of new chiral centers. This makes 1,3-Dimethyladamantane a valuable tool in the synthesis of enantiopure compounds, which are crucial in the pharmaceutical industry for the development of drugs with specific biological activity and minimal side effects.Additionally, 1,3-Dimethyladamantane can be used as a protecting group in organic synthesis to shield reactive functional groups from unwanted side reactions. By strategically introducing and removing the 1,3-Dimethyladamantane moiety, chemists can selectively manipulate the reactivity of key functional groups, enabling the synthesis of complex molecules with high efficiency and selectivity.Overall, the incorporation of 1,3-Dimethyladamantane in chemical synthesis strategies offers a powerful and reliable approach to achieve precise control over stereochemistry and reactivity, facilitating the efficient production of structurally diverse and biologically active compounds.

Literature

• The rate of removal and the compositional changes of diesel in Antarctic marine sediment.

  The Science of the total environment 20111201

• Catalytic oxyalkylation of alkenes with alkanes and molecular oxygen via a radical process using N-hydroxyphthalimide.

  The Journal of organic chemistry 20010921