184209
1-Adamantanemethanol
99%
Synonym(s):
1-(Hydroxymethyl)adamantane
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About This Item
Empirical Formula (Hill Notation):
C11H18O
CAS Number:
Molecular Weight:
166.26
EC Number:
212-225-3
UNSPSC Code:
12352100
PubChem Substance ID:
Beilstein/REAXYS Number:
1853339
MDL number:
InChI key
MDVGOOIANLZFCP-BIBSGERRSA-N
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-
SMILES string
OCC12C[C@H]3C[C@H](C[C@H](C3)C1)C2
assay
99%
form
solid
General description
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.
Application
1-Adamantanemethanol was used in the synthesis of axially disubstituted silicon(IV) phthalocyanines.
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
Regulatory Information
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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
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
Roman S Borisov et al.
Talanta, 200, 31-40 (2019-05-01)
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
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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