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| | 1-Bromoadamantane Basic information |
| Product Name: | 1-Bromoadamantane | | Synonyms: | 1-Bromoadamantane,99%;11 -BROMOADAMANTANE;3-Bromoadamantane;1-Bromoadamantane,1-Adamantyl bromide;1-BroMoadaMantan;1-broMine adaMantanone;1-BROMOADAMANTANE FOR SYNTHESIS;1-broMideadaMantane | | CAS: | 768-90-1 | | MF: | C10H15Br | | MW: | 215.13 | | EINECS: | 212-200-7 | | Product Categories: | Adamantanes;768-90-1 | | Mol File: | 768-90-1.mol |  |
| | 1-Bromoadamantane Chemical Properties |
| Melting point | 116-118 °C (lit.) | | Boiling point | 248.79°C (rough estimate) | | density | 1.2686 (rough estimate) | | refractive index | 1.6411 (estimate) | | storage temp. | Inert atmosphere,Room Temperature | | solubility | Chloroform (Sparingly), Ethyl Acetate (Slightly), Methanol (Slightly) | | form | Powder | | color | White to yellow | | Water Solubility | It is soluble in organic solvents and insoluble in water. | | Sensitive | Moisture Sensitive | | BRN | 1098857 | | InChIKey | VQHPRVYDKRESCL-UHFFFAOYSA-N | | CAS DataBase Reference | 768-90-1(CAS DataBase Reference) | | NIST Chemistry Reference | 1-Bromoadamantane(768-90-1) |
| | 1-Bromoadamantane Usage And Synthesis |
| Chemical Properties | WHITE TO ALMOST WHITE CRYSTALS OR CRYST. POWDER | | Uses | 1-Bromoadamantane shows some anti-viral activity due to the adamantane structure. In addition it shows anti-microbial activity and cytotoxic application.
| | Uses | 1-Bromoadamantane is an important intermediate, used in synthesizing medicines and new materials etc. | | Uses | use: Amantadine, Rimantadine, Somantadine, Tromantadine | | Application | 1-Bromoadamantane was used in the synthesis of a new organic–organic nanoscale composite thin-film dielectric.
1-Bromoadamantane forms inclusion complexes with α-, β-, and γ-cyclodextrins. It causes the alkylation of Co(II) complexes of β-diketones. | | Synthesis Reference(s) | The Journal of Organic Chemistry, 45, p. 5239, 1980 DOI: 10.1021/jo01314a003 | | General Description | 1-Bromoadamantane forms inclusion complexes with α-, β-, and γ-cyclodextrins. It causes the alkylation of Co(II) complexes of β-diketones. | | Purification Methods | If coloured, dissolve it in CCl4, wash with H2O, treat with charcoal, dry (CaCl2), filter and evaporate to dryness. Dissolve the residue in a small volume of MeOH and cool in a CO2/trichloroethylene bath and collect the crystals. Sublime it at 90-100o/water pump vacuum. [Stetter et al. Chem Ber 92 1629 1959, Schleyer & Nicholas J Am Chem Soc 83 2700 1961, Beilstein 5 III 469.] |
| | 1-Bromoadamantane Preparation Products And Raw materials |
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