Adamantane - CAS 281-23-2
Catalog: |
BB019771 |
Product Name: |
Adamantane |
CAS: |
281-23-2 |
Synonyms: |
adamantane |
Application: |
building blocks |
IUPAC Name: | adamantane |
Description: | 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 consist of four connected cyclohexane rings arranged in the "armchair" configuration. It is unique in that it is both rigid and virtually stress-free. A boat-shaped configuration can also exist. Adamantane is the most stable among all the isomers with formula C10H16, which include the somewhat similar twistane. The spatial arrangement of carbon atoms in adamantane molecule is the same as in the diamond crystal. This motivates the name adamantane, which is derived from the Greek adamantinos (relating to steel or diamond).The discovery of adamantane in petroleum in 1933 launched a new field of chemistry dedicated to studying the synthesis and properties of polyhedral organic compounds. Adamantane derivatives have found practical application as drugs, polymeric materials and thermally stable lubricants. |
Molecular Weight: | 136.23 |
Molecular Formula: | C10H16 |
Canonical SMILES: | C1C2CC3CC1CC(C2)C3 |
InChI: | InChI=1S/C10H16/c1-7-2-9-4-8(1)5-10(3-7)6-9/h7-10H,1-6H2 |
InChI Key: | ORILYTVJVMAKLC-UHFFFAOYSA-N |
Boiling Point: | 187.1 °C at 760 mmHg |
Melting Point: | 183-186 °C |
Purity: | > 98 % |
Density: | 1.08 g/cm3 (20 °C) |
Appearance: | Colorless, crystalline |
MDL: | MFCD00074719 |
LogP: | 2.83260 |
GHS Hazard Statement: | H319 (13.21%): Causes serious eye irritation [Warning Serious eye damage/eye irritation]; H400 (96.23%): Very toxic to aquatic life [Warning Hazardous to the aquatic environment, acute hazard] |
Precautionary Statement: | P264+P265, P273, P280, P305+P351+P338, P337+P317, P391, and P501 |
Signal Word: | Warning |
Publication Number | Title | Priority Date |
WO-2021201227-A1 | Resin, resin precursor composition, coating composition, electrophotographic photoreceptor, electrophotographic photoreceptor production method, molded article, and electronic device | 20200401 |
WO-2021201228-A1 | Resin, resin precursor composition, coating composition, electrophotographic photoreceptor, molded article, electronic device, and electrophotographic photoreceptor production method | 20200401 |
WO-2021198855-A1 | Low temperature foamable flame retardant polycarbonate composition | 20200331 |
JP-2021155499-A | Resin composition and molded product | 20200325 |
US-2021292559-A1 | Additive manufacturing method and associated article | 20200323 |
PMID | Publication Date | Title | Journal |
32345068 | 20200601 | Peficitinib for the treatment of rheumatoid arthritis: an overview from clinical trials | Expert opinion on pharmacotherapy |
32589689 | 20200601 | System-wide biochemical analysis reveals ozonide antimalarials initially act by disrupting Plasmodium falciparum haemoglobin digestion | PLoS pathogens |
31629700 | 20200105 | Saxagliptin protects against hypoxia-induced damage in H9c2 cells | Chemico-biological interactions |
31093950 | 20190601 | Peficitinib: First Global Approval | Drugs |
30735041 | 20190306 | Cryptic and Stereospecific Hydroxylation, Oxidation, and Reduction in Platensimycin and Platencin Biosynthesis | Journal of the American Chemical Society |
Complexity: | 75.1 |
Compound Is Canonicalized: | Yes |
Covalently-Bonded Unit Count: | 1 |
Defined Atom Stereocenter Count: | 0 |
Defined Bond Stereocenter Count: | 0 |
Exact Mass: | 136.12520051 |
Formal Charge: | 0 |
Heavy Atom Count: | 10 |
Hydrogen Bond Acceptor Count: | 0 |
Hydrogen Bond Donor Count: | 0 |
Isotope Atom Count: | 0 |
Monoisotopic Mass: | 136.12520051 |
Rotatable Bond Count: | 0 |
Topological Polar Surface Area: | 0 |
Undefined Atom Stereocenter Count: | 0 |
Undefined Bond Stereocenter Count: | 0 |
XLogP3: | 3.8 |
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