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1-Adamantanmethanol
99%
Synonym(e):
1-Adamantylmethanol
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About This Item
Empirische Formel (Hill-System):
C11H18O
CAS-Nummer:
Molekulargewicht:
166.26
Beilstein:
1853339
EG-Nummer:
MDL-Nummer:
UNSPSC-Code:
12352100
PubChem Substanz-ID:
Empfohlene Produkte
Assay
99%
Form
solid
mp (Schmelzpunkt)
114-117 °C (lit.)
SMILES String
OCC12C[C@H]3C[C@H](C[C@H](C3)C1)C2
InChI
1S/C11H18O/c12-7-11-4-8-1-9(5-11)3-10(2-8)6-11/h8-10,12H,1-7H2/t8-,9+,10-,11-
InChIKey
MDVGOOIANLZFCP-BIBSGERRSA-N
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Allgemeine Beschreibung
1-Adamantanemethanol acts as guest molecule and forms β-cyclodextrin complexes. It reacts with 3,4,5,6-tetrafluorophthalonitrile to yield 3,4,5,6-tetra-(1-adamantylmethoxy)phthalonitrile.
Anwendung
1-Adamantanemethanol was used in the synthesis of axially disubstituted silicon(IV) phthalocyanines.
Lagerklassenschlüssel
11 - Combustible Solids
WGK
WGK 3
Flammpunkt (°F)
Not applicable
Flammpunkt (°C)
Not applicable
Persönliche Schutzausrüstung
Eyeshields, Gloves, type N95 (US)
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A S Kostense et al.
Journal of computer-aided molecular design, 5(6), 525-543 (1991-12-01)
A series of beta-cyclodextrin complexes containing various guest molecules was studied using computer-aided molecular modeling and conformation analysis techniques. The geometry of each complex was studied using crystallographic data. The positions of the glycosidic O4 atoms indicate that the beta-cyclodextrin
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Syntheses and characterization of phthalonitriles and phthalocyanines substituted with adamantane moieties.
Causey PW, et al.
Canadian Journal of Chemistry, 84(10), 1380-1387 (2006)
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Analytical and bioanalytical chemistry (2018-07-15)
A sensitive competitive immunoassay with simple operation was developed for the detection of the anti-virus drug amantadine (AMD). The single-chain variable fragment (scFv) antibody against AMD was site-specific biotinylated and overexpressed as a secreted body in Escherichia coli AVB101. Horseradish
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This work highlights the discovered in-situ analytical reaction between primary/secondary alcohols and nitrogenous bases (pyridine, quinoline) that involves the substitution of hydroxyl groups for nitrogen-containing charged species and proceeds in an ionization region of Direct Analysis in Real Time mass
Unser Team von Wissenschaftlern verfügt über Erfahrung in allen Forschungsbereichen einschließlich Life Science, Materialwissenschaften, chemischer Synthese, Chromatographie, Analytik und vielen mehr..
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