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Merck
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423807

Sigma-Aldrich

5-羟基-2-金刚烷酮

98%

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About This Item

经验公式（希尔记法）:
C10H14O2
CAS号:
20098-14-0
分子量:
166.22
MDL编号:
MFCD00192211
UNSPSC代码:
12352100
PubChem化学物质编号:
24866531
NACRES:
NA.22

方案

98%

表单

solid

mp

>300 °C (lit.)

官能团

hydroxyl
ketone

SMILES字符串

O[C@]12C[C@@H]3C[C@H](C1)C(=O)[C@@H](C3)C2

InChI

1S/C10H14O2/c11-9-7-1-6-2-8(9)5-10(12,3-6)4-7/h6-8,12H,1-5H2/t6-,7-,8+,10-

InChI key

TZBDEVBNMSLVKT-XYYXLIQBSA-N

一般描述

5-Hydroxy-2-adamantanone is a disubstituted derivative of adamantane.[1] The biocatalyzed synthesis of 5-hydroxy-2-adamantanone from 2-adamantanone has been investigated.[2]

应用

5-Hydroxy-2-adamantanone may be used in the following studies:
  • As a model compound to investigate the application of lanthanide NMR shift reagents for the analysis of disubstituted derivative of adamantane.[1]
  • As a starting material for the synthesis of E-2-amino-5-hydroxyadamantane.[3]
  • As a starting material for the synthesis of 4-(triphenylsilyloxy)adamantan-1-ol.[4]

储存分类代码

11 - Combustible Solids

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

Eyeshields, Gloves, type N95 (US)

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number
MKCN0955
MKBC8866
MKAA2767
00818AJ
05811JE

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Biocatalytic production of 5-hydroxy-2-adamantanone by P450cam coupled with NADH regeneration.
Furuya T, et al.
Journal of Molecular Catalysis. B, Enzymatic, 94, 111-118 (2013)
S S Boĭko et al.
Eksperimental'naia i klinicheskaia farmakologiia, 57(6), 48-50 (1994-11-01)
The pharmacokinetics of the new immunostimulant kemantane, adamantane derivative, used in two species of animals (rats and rabbits) and man was studied. There were significant differences in the pharmacokinetics of kemantane and its active metabolite--adamantane-1,4-diol between the species.
V M Man'ko et al.
Zhurnal mikrobiologii, epidemiologii, i immunobiologii, (9)(9), 66-67 (1991-09-01)
The study of Kemantan on functionally alternative humoral immunity regulator cells: T-helpers and antigen-specific T-suppressors, including their induction, accumulation and functioning, was studied. Kemantan in doses of 0.2-200 mg/kg, introduced to the donors of T-helpers 2 days before they were
Application of shift reagents in the study of disubstituted derivatives of adamantane by NMR spectroscopy.
Vodicka L, et al.
Collection of Czechoslovak Chemical Communications, 40(1), 293-299 (1975)
N V Kossii et al.
Problemy tuberkuleza, (6)(6), 23-26 (1991-01-01)
Observation of 219 patients with pulmonary tuberculosis was made to study the effect of acute respiratory viral infection (ARVI) on the course of the disease. The affected were divided into 2 groups: 136 subjects who had ARVI and 83 persons
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