ChemicalBook > CAS DataBase List > 5-Hydroxyadamantan-2-one

5-Hydroxyadamantan-2-one

Product Name
5-Hydroxyadamantan-2-one
CAS No.
20098-14-0
Chemical Name
5-Hydroxyadamantan-2-one
Synonyms
HADON;kemantane;AKOS BB-9629;CHEMBRDG-BB 4013898;Hydroxyadamantanone;Adamantan-4-on-1-ol;5-Hydroxy-2-adamantone;Kemantane( Idramantone);5-HYDROXY-2-ADAMANTANONE;5-Hydroxyadamantan-2-one
CBNumber
CB5361850
Molecular Formula
C10H14O2
Formula Weight
166.22
MOL File
20098-14-0.mol
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5-Hydroxyadamantan-2-one Property

Melting point:
>300 °C (lit.)
Boiling point:
296.5±33.0 °C(Predicted)
Density 
1.301±0.06 g/cm3(Predicted)
storage temp. 
Sealed in dry,Room Temperature
solubility 
DMSO, Methanol
pka
14.69±0.20(Predicted)
form 
Crystalline Powder
color 
White to off-white
InChI
InChI=1S/C10H14O2/c11-9-7-1-6-2-8(9)5-10(12,3-6)4-7/h6-8,12H,1-5H2
InChIKey
TZBDEVBNMSLVKT-RIKBPLFRSA-N
SMILES
C12CC3(O)CC(CC(C3)C1=O)C2
CAS DataBase Reference
20098-14-0(CAS DataBase Reference)
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Safety

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
24/25-36/37/39-27-26
WGK Germany 
3
HazardClass 
IRRITANT
HS Code 
29144000
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H302Harmful if swallowed

H315Causes skin irritation

H319Causes serious eye irritation

H335May cause respiratory irritation

Precautionary statements

P261Avoid breathing dust/fume/gas/mist/vapours/spray.

P271Use only outdoors or in a well-ventilated area.

P280Wear protective gloves/protective clothing/eye protection/face protection.

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N-Bromosuccinimide Price

Sigma-Aldrich
Product number
423807
Product name
5-Hydroxy-2-adamantanone
Purity
98%
Packaging
1g
Price
$26.3
Updated
2023/06/20
TCI Chemical
Product number
H0962
Product name
5-Hydroxy-2-adamantanone
Purity
>98.0%(GC)
Packaging
1g
Price
$34
Updated
2025/07/31
TCI Chemical
Product number
H0962
Product name
5-Hydroxy-2-adamantanone
Purity
>98.0%(GC)
Packaging
5g
Price
$130
Updated
2025/07/31
TCI Chemical
Product number
H0962
Product name
5-Hydroxy-2-adamantanone
Purity
>98.0%(GC)
Packaging
25g
Price
$386
Updated
2025/07/31
Usbiological
Product number
161910
Product name
5-Hydroxy-2-adamantanone
Packaging
2.5g
Price
$403
Updated
2021/12/16
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5-Hydroxyadamantan-2-one Chemical Properties,Usage,Production

Description

5-Hydroxy-2-adamantanone (5-hydroxyadamantan-2-one) is a versatile starting material for synthesising various 2,5- or 1,4-disubstituted adamantanes. Chemical methods for synthesizing 5-hydroxy-2-adamantanone include disproportionation of 2-hydroxyadamantane and oxidation of 2-adamantanone. A synthetic approach to produce 5-hydroxy-2-adamantanone using P450cam (CYP101A1; a camphor monooxygenase) coupled with NADH regeneration as an oxidation biocatalyst has been reported[1].

Chemical Properties

White crystal or crystalline powder

Uses

anthelmintic

Uses

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.
  • As a starting material for the synthesis of E-2-amino-5-hydroxyadamantane.
  • As a starting material for the synthesis of 4-(triphenylsilyloxy)adamantan-1-ol.

Definition

ChEBI: Idramantone is a member of adamantanones.

brand name

INDICLOR (Nycomed Amersham).

General Description

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

Synthesis

700-58-3

20098-14-0

Step (i): Synthesis of 5-hydroxy-2-adamantanone (compound of formula 11) Under cooling in an ice bath, adamantanone (50 g, 333 mmol) was slowly added to concentrated nitric acid (98%, 440 mL) for 15 min while stirring was maintained. The reaction mixture was stirred continuously for 72 h at room temperature and then warmed to 60 °C for 2 h until most of the nitrogen dioxide gas escaped. Excess nitric acid was removed by distillation under reduced pressure and the resulting pale yellow oil solidified on cooling. The reaction mixture was sequentially diluted with deionized water (200 mL) and concentrated sulfuric acid (75 mL), and the resulting clarified yellow solution was heated on a steam bath in a fume hood for 1 hour. The reaction solution was neutralized with 30% aqueous sodium hydroxide under warm conditions and subsequently extracted with chloroform. The organic phases were combined, washed with saturated saline and concentrated under reduced pressure. The crude product was dissolved in dichloromethane (15 mL), hexane was added dropwise until the precipitate was no longer generated, the solid was collected by filtration and dried under vacuum to give 5-hydroxy-2-adamantanone (compound of formula 11, 40.9 g) in 74% yield. Characterization data: Melting point: 278.8-300°C; 1H-NMR (CDCl3) δ: 2.69 (bs, 2H), 2.36-2.32 (m, 2H), 2.12-2.02 (m, 2H), 2.02-1.88 (m, 6H), 1.80-1.68 (m, 1H); IR (cm-1): 3410, 2929, 2855, 2645, 1725, 1539, 1452, 1351, 1288, 1116, 1055, 927, 900, 797; Mass spectrum (m/z): 167 [M+H]+.

References

[1] Toshiki Furuya . “Biocatalytic production of 5-hydroxy-2-adamantanone by P450cam coupled with NADH regeneration.” Journal of Molecular Catalysis B-enzymatic 94 (2013): Pages 111-118.

5-Hydroxyadamantan-2-one Preparation Products And Raw materials

Raw materials

Preparation Products

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5-Hydroxyadamantan-2-one Suppliers

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View Lastest Price from 5-Hydroxyadamantan-2-one manufacturers

Dideu Industries Group Limited
Product
5-Hydroxyadamantan-2-one 20098-14-0
Price
US $1.10/g
Min. Order
1g
Purity
99.9%
Supply Ability
100 Tons Min
Release date
2025-09-17
Wuhan JiyunZen Tech Co., Ltd.
Product
5-Hydroxyadamantan-2-one 20098-14-0
Price
US $5.00-0.50/KG
Min. Order
1KG
Purity
99% hplc
Supply Ability
500TONS
Release date
2025-05-30
Shanghai Qyubiotech Co., Ltd.
Product
5-Hydroxy-2-adamantanone 20098-14-0
Price
US $0.00-0.00/kg
Min. Order
1kg
Purity
98%+
Supply Ability
1000kg per Month
Release date
2023-08-11

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