184209
1-Adamantanemethanol
99%
Sinônimo(s):
1-(Hydroxymethyl)adamantane
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About This Item
Fórmula empírica (Notação de Hill):
C11H18O
Número CAS:
Peso molecular:
166.26
Beilstein:
1853339
Número CE:
Número MDL:
Código UNSPSC:
12352100
ID de substância PubChem:
Produtos recomendados
Ensaio
99%
Formulário
solid
pf
114-117 °C (lit.)
cadeia de caracteres SMILES
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-
chave InChI
MDVGOOIANLZFCP-BIBSGERRSA-N
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Descrição geral
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.
Aplicação
1-Adamantanemethanol was used in the synthesis of axially disubstituted silicon(IV) phthalocyanines.
Código de classe de armazenamento
11 - Combustible Solids
Classe de risco de água (WGK)
WGK 3
Ponto de fulgor (°F)
Not applicable
Ponto de fulgor (°C)
Not applicable
Equipamento de proteção individual
Eyeshields, Gloves, type N95 (US)
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Jan Chyba et al.
Inorganic chemistry, 57(15), 8735-8747 (2018-04-06)
The potential of paramagnetic ruthenium(III) compounds for use as anticancer metallodrugs has been investigated extensively during the past several decades. However, the means by which these ruthenium compounds are transported and distributed in living bodies remain relatively unexplored. In this
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
Syntheses and characterization of phthalonitriles and phthalocyanines substituted with adamantane moieties.
Causey PW, et al.
Canadian Journal of Chemistry, 84(10), 1380-1387 (2006)
Sanlei Xie et al.
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
Highly photostable silicon (IV) phthalocyanines containing adamantane moieties: synthesis, structure, and properties.
Shen X-M, et al.
Tetrahedron, 66(46), 9041-9048 (2010)
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