768-93-4
Chemical Structure
1-Iodoadamantane
- CAS No.: 768-93-4
- Formula:C10H15I
- Molecular Weight:262.13
IUPAC Name: 1-iodoadamantane
InChIKey: PXVOATXCSSPUEM-UHFFFAOYSA-N
SMILES: IC1(C2)CC3CC2CC(C3)C1
Biological Activity: 1-Iodoadamantane is a 1-substituted adamantane derivative. On a silver electrode in aprotic solvents, 1-Iodoadamantane can be reduced to form a mixture of adamantane and 1,1'-biadamantane without insonation, while only adamantane is formed under the action of 10 kHz insonation[1][2].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
|
1-Iodoadamantane | 1-Iodoadamantane is a 1-substituted adamantane derivative. On a silver electrode in aprotic solvents, 1-Iodoadamantane can be reduced to form a mixture of adamantane and 1,1'-biadamantane without insonation, while only adamantane is formed under the action of 10 kHz insonation. | |||||||||||||||||||||
|
loading...
/
|
|||||||||||||||||||||||
- [1]. Jain MK, et al. Phase transition in a lipid bilayer. II. Influence of adamantane derivatives. Chem Phys Lipids. 1976 Sep;17(1):71-8. [Content Brief]
- [2]. Paddon CA, et al. Electrosynthetic reduction of 1-iodoadamantane forming 1,1'-biadamantane and adamantane in aprotic solvents: insonation switches the mechanism from dimerisation to exclusive monomer formation. Ultrason Sonochem. 2007 Jul;14(5):502-508. [Content Brief]
Keywords