153826
2-金刚烷醇
97%
别名:
2-羟基金刚烷
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关于此项目
经验公式（希尔记法）:
C10H16O
化学文摘社编号:
分子量:
152.23
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
211-846-7
Beilstein/REAXYS Number:
2498536
MDL number:
产品名称
2-金刚烷醇, 97%
InChI key
FOWDOWQYRZXQDP-MGPGSJOLSA-N
InChI
1S/C10H16O/c11-10-8-2-6-1-7(4-8)5-9(10)3-6/h6-11H,1-5H2/t6-,7+,8-,9+,10?
SMILES string
OC1[C@H]2C[C@@H]3C[C@H](C2)C[C@H]1C3
assay
97%
form
solid
mp
258-262 °C (lit.)
functional group
hydroxyl
Quality Level
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Application
2-Adamantanol was used to synthesize ester imides.
General description
The low-temperature X-ray structure of 2-adamantanol ester has been studied.
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
Andrzej Orzeszko et al.
Farmaco (Societa chimica italiana : 1989), 57(8), 619-624 (2002-10-04)
Some novel ester imides synthesised from trimellitic acid anhydride and 1-adamantanol or 2-adamantanol, were tested as antimicrobial compounds. Unfortunately, these agents showed a modest antibacterial activity (MIC > 6 microg/ml). However, a comparison of these N-substituted adamantylester imides with the
J P Miller et al.
Biochemistry, 33(3), 807-817 (1994-01-25)
Spiro[adamantane-2,2'-diazirine], which produces adamantyl carbene upon photolysis, binds tightly to P450 2B4 (KS = 3.2 microM), giving a normal substrate binding difference spectrum. Irradiation of 2-[3H]adamantane diazirine at 365 nm in the presence of native, ferric P450 2B4 resulted in
T Mavromoustakos et al.
Life sciences, 62(20), 1901-1910 (1998-05-26)
Differential Scanning Calorimetry (DSC) has been applied to study the thermal properties of the membrane perturbing antibacterial octyl- and dodecyl-bromide salts of quaternary dimethylamino adamantanol (ADM-8 and ADM-12 correspondingly) incorporated in free or complexed form with beta-cyclodextrin (beta-CD) into dipalmitoylphosphatidylcholine
Koichi Mitsukura et al.
Applied microbiology and biotechnology, 71(4), 502-504 (2005-09-28)
Hydroxylation of adamantane using whole cells of bacteria, actinomyces, and molds was examined. The structure of the product was determined using gas chromatography (GC), nuclear magnetic resonance (NMR), and mass spectroscopy (MS). Among 470 strains tested, Streptomyces griseoplanus was highly
Marisa Spiniello et al.
Organic & biomolecular chemistry, 1(17), 3094-3101 (2003-10-02)
Results of low-temperature X-ray structural studies for five cis-, and three trans-4-tert-butyl cyclohexanol, and six 2-adamantanol ester and ether derivatives are reported. Plots of C-OR bond distance against pKa(ROH) for derivatives of axial alcohol (5), equatorial alcohol (6) and 2-adamantanol
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