2-Adamantanol - CAS 700-57-2
Catalog: |
BB034058 |
Product Name: |
2-Adamantanol |
CAS: |
700-57-2 |
Synonyms: |
Tricyclo[3.3.1.13,7]decan-2-ol; 2-Hydroxyadamantane; 2-Tricyclo[3.3.1.13,7]decanol; NSC 193480 |
IUPAC Name: | adamantan-2-ol |
Description: | Used in make adamantane derivatives and other pharmaceutical intermediates. |
Molecular Weight: | 152.23 |
Molecular Formula: | C10H16O |
Canonical SMILES: | C1C2CC3CC1CC(C2)C3O |
InChI: | InChI=1S/C10H16O/c11-10-8-2-6-1-7(4-8)5-9(10)3-6/h6-11H,1-5H2 |
InChI Key: | FOWDOWQYRZXQDP-UHFFFAOYSA-N |
Boiling Point: | 255.2±8.0°C at 760 mmHg |
Melting Point: | 296-300°C |
Purity: | ≥95% |
Density: | 1.115±0.06 g/cm3 |
Solubility: | Soluble in Methanol |
Appearance: | White to off-white crystalline powder |
Storage: | Store at RT |
MDL: | MFCD00074744 |
LogP: | 1.80340 |
Publication Number | Title | Priority Date |
EP-3828630-A1 | Material for forming organic film, patterning process, and polymer | 20191128 |
US-2021163675-A1 | Material for forming organic film, patterning process, and polymer | 20191128 |
WO-2021103798-A1 | Method for preparing lactone compound | 20191128 |
WO-2021079856-A1 | Organic electroluminescent element | 20191023 |
WO-2021070878-A1 | Organic electroluminescence element having organic layer comprising high molecular weight compound | 20191009 |
PMID | Publication Date | Title | Journal |
22008723 | 20111201 | Sterically congested quinone methides in photodehydration reactions of 4-hydroxybiphenyl derivatives and investigation of their antiproliferative activity | Photochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology |
21850329 | 20111007 | Nickel(II) complexes of tripodal 4N ligands as catalysts for alkane oxidation using m-CPBA as oxidant: ligand stereoelectronic effects on catalysis | Dalton transactions (Cambridge, England : 2003) |
20864344 | 20101115 | Discovery and optimization of adamantyl carbamate inhibitors of 11β-HSD1 | Bioorganic & medicinal chemistry letters |
20471592 | 20100601 | Bioconversion of 1-adamantanol to 1,3-adamantanediol using Streptomyces sp. SA8 oxidation system | Journal of bioscience and bioengineering |
19957924 | 20100101 | Photochemical formation and chemistry of long-lived adamantylidene-quinone methides and 2-adamantyl cations | The Journal of organic chemistry |
Complexity: | 148 |
Compound Is Canonicalized: | Yes |
Covalently-Bonded Unit Count: | 1 |
Defined Atom Stereocenter Count: | 0 |
Defined Bond Stereocenter Count: | 0 |
Exact Mass: | 152.12011513 |
Formal Charge: | 0 |
Heavy Atom Count: | 11 |
Hydrogen Bond Acceptor Count: | 1 |
Hydrogen Bond Donor Count: | 1 |
Isotope Atom Count: | 0 |
Monoisotopic Mass: | 152.12011513 |
Rotatable Bond Count: | 0 |
Topological Polar Surface Area: | 20.2 |
Undefined Atom Stereocenter Count: | 0 |
Undefined Bond Stereocenter Count: | 0 |
XLogP3: | 1.9 |
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