| Weight | 136.238 g/mol |
|---|---|
| Formula | C10H16 |
| Hydrogen Acceptors | 0 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 0 |
ADAMANTANE (281-23-2)
Diamantane
Score:
#1886 in Physics
,
#5885 in Chemistry
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- Incidence of adamantane resistance among influenza A (H3N2) viruses isolated worldwide from 1994 to 2005: a cause for concern. (The Lancet, 2005)
- Adamantane Resistance Among Influenza A Viruses Isolated Early During the 2005-2006 Influenza Season in the United States (JAMA, 2006)
- Evaluation of strain in hydrocarbons. The strain in adamantane and its origin (Journal of the American Chemical Society, 1970)
- Cu2(ATC)6H2O: Design of Open Metal Sites in Porous MetalOrganic Crystals (ATC: 1,3,5,7-Adamantane Tetracarboxylate) (Journal of the American Chemical Society, 2000)
- Adamantane: Consequences of the Diamondoid Structure (Chemical Reviews, 1964)
- Five-fold diamond structure of adamantane-1,3,5,7-tetracarboxylic acid (Journal of the American Chemical Society, 1988)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - Diamantane
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SMILESC1C2CC3CC1CC(C2)C3
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InChIKeyORILYTVJVMAKLC-UHFFFAOYSA-N
- Pubchem - ADAMANTANE
- Wikipedia - adamantane
Adamantane is a colorless, crystalline chemical compound with a camphor-like odor. With a formula C10H16, it is a cycloalkane and also the simplest diamondoid. Adamantane molecules consists of three connected cyclohexane rings arranged in the "armchair" configuration.
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ADAMANTANE
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