2-Adamantanone - CAS 700-58-3
Catalog: |
BB034062 |
Product Name: |
2-Adamantanone |
CAS: |
700-58-3 |
Synonyms: |
adamantan-2-one |
Application: |
building blocks |
IUPAC Name: | adamantan-2-one |
Description: | Used to produce pharmaceutical intermediate,photosensitive material and informational technology range. |
Molecular Weight: | 150.22 |
Molecular Formula: | C10H14O |
Canonical SMILES: | C1C2CC3CC1CC(C2)C3=O |
InChI: | InChI=1S/C10H14O/c11-10-8-2-6-1-7(4-8)5-9(10)3-6/h6-9H,1-5H2 |
InChI Key: | IYKFYARMMIESOX-UHFFFAOYSA-N |
Boiling Point: | 246.7 °C at 760 mmHg |
Purity: | > 98 % |
Density: | 1.105 g/cm3 |
Appearance: | White to offwhite crystalline powder |
MDL: | MFCD00074737 |
LogP: | 2.01160 |
GHS Hazard Statement: | H301 (33.33%): Toxic if swallowed [Danger Acute toxicity, oral] |
Precautionary Statement: | P264, P270, P273, P280, P301+P310, P302+P352, P305+P351+P338, P310, P321, P330, P332+P313, P362, P391, P405, and P501 |
Signal Word: | Danger |
Publication Number | Title | Priority Date |
CN-113045434-A | Organic compound, and organic electroluminescent device and electronic device using same | 20210303 |
CN-112939880-A | Organic compound, and electronic element and electronic device using same | 20210210 |
CN-113024523-A | Chemiluminescent probe for detecting fibroblast activation protein and synthetic method and application thereof | 20210208 |
CN-112812010-A | Method for synthesizing adamantane ester (methyl) acrylate | 20201228 |
CN-112661637-A | Degradable resin monomer synthesized from adamantanone and preparation method thereof | 20201223 |
PMID | Publication Date | Title | Journal |
22717441 | 20120603 | Mechanically induced chemiluminescence from polymers incorporating a 1,2-dioxetane unit in the main chain | Nature chemistry |
22587703 | 20120601 | Cucurbituril adamantanediazirine complexes and consequential carbene chemistry | The Journal of organic chemistry |
22220129 | 20111101 | N'-(Adamantan-2-yl-idene)thio-phene-2-carbohydrazide | Acta crystallographica. Section E, Structure reports online |
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) |
21186391 | 20110401 | Spring-loading the active site of cytochrome P450cam | Metallomics : integrated biometal science |
Complexity: | 177 |
Compound Is Canonicalized: | Yes |
Covalently-Bonded Unit Count: | 1 |
Defined Atom Stereocenter Count: | 0 |
Defined Bond Stereocenter Count: | 0 |
Exact Mass: | 150.104465066 |
Formal Charge: | 0 |
Heavy Atom Count: | 11 |
Hydrogen Bond Acceptor Count: | 1 |
Hydrogen Bond Donor Count: | 0 |
Isotope Atom Count: | 0 |
Monoisotopic Mass: | 150.104465066 |
Rotatable Bond Count: | 0 |
Topological Polar Surface Area: | 17.1 Å2 |
Undefined Atom Stereocenter Count: | 0 |
Undefined Bond Stereocenter Count: | 0 |
XLogP3: | 1.8 |
Online Inquiry
Customer Support
Customer Centered
Related Functional Groups
Carbonyl Compounds
Customers Also Viewed
INDUSTRY LEADERS TRUST OUR PRODUCTS