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153826

2-Adamantanol

97%

Synonym(s):

2-Hydroxyadamantane

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About This Item

Empirical Formula (Hill Notation):
C10H16O
CAS Number:
700-57-2
Molecular Weight:
152.23
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
24849378
EC Number:
211-846-7
Beilstein/REAXYS Number:
2498536
MDL number:
MFCD00074744
Assay:
97%
Form:
solid
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Quality Level

100

assay

97%

form

solid

mp

258-262 °C (lit.)

functional group

hydroxyl

SMILES string

OC1[C@H]2C[C@@H]3C[C@H](C2)C[C@H]1C3

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?

InChI key

FOWDOWQYRZXQDP-MGPGSJOLSA-N

General description

The low-temperature X-ray structure of 2-adamantanol ester has been studied.

Application

2-Adamantanol was used to synthesize ester imides.

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

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Certificates of Analysis (COA)

Lot/Batch Number
MKBC0014
07604AH
10207TE
11102PE
12008LE

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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
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
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
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Global Trade Item Number

SKUGTIN
153826-5G04061832278704