![]() adamantanone structure
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Common Name | adamantanone | ||
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CAS Number | 700-58-3 | Molecular Weight | 150.218 | |
Density | 1.1±0.1 g/cm3 | Boiling Point | 246.7±8.0 °C at 760 mmHg | |
Molecular Formula | C10H14O | Melting Point | 256-258 °C (subl.)(lit.) | |
MSDS | Chinese USA | Flash Point | 95.7±10.7 °C |
Use of adamantanoneAdamantanone (2-Adamantone) is a bioactive chemical, and can be used for the synthesis of active compound[1]. |
Name | adamantanone |
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Synonym | More Synonyms |
Description | Adamantanone (2-Adamantone) is a bioactive chemical, and can be used for the synthesis of active compound[1]. |
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Related Catalog |
Density | 1.1±0.1 g/cm3 |
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Boiling Point | 246.7±8.0 °C at 760 mmHg |
Melting Point | 256-258 °C (subl.)(lit.) |
Molecular Formula | C10H14O |
Molecular Weight | 150.218 |
Flash Point | 95.7±10.7 °C |
Exact Mass | 150.104462 |
PSA | 17.07000 |
LogP | 1.60 |
Vapour Pressure | 0.0±0.5 mmHg at 25°C |
Index of Refraction | 1.535 |
Water Solubility | methanol: 0.1 g/mL, clear |
CHEMICAL IDENTIFICATION
HEALTH HAZARD DATAACUTE TOXICITY DATA
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Personal Protective Equipment | Eyeshields;Gloves |
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Hazard Codes | Xi: Irritant; |
Risk Phrases | R52 |
Safety Phrases | S22-S24/25 |
RIDADR | NONH for all modes of transport |
WGK Germany | 2 |
RTECS | AU5018000 |
HS Code | 29142900 |
Precursor 9 | |
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DownStream 9 | |
HS Code | 2914299000 |
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Summary | 2914299000. other cyclanic, cyclenic or cyclotherpenic ketones without other oxygen function. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:5.5%. General tariff:30.0% |
Effect of adamantanone derivative possessing anti-HIV properties on the redox processes in the cytochrome P-450 system.
Dokl. Biochem. Biophys. 378 , 210-3, (2001)
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Conformational relaxation in hemoproteins: the cytochrome P-450cam case.
Biochemistry 39(46) , 14219-31, (2000) Photodissociation of (CO)P-450(cam)(substrate) complexes was found to trigger a conformational relaxation process that interferes with ligand rebinding at temperatures as low as 140 K even though the ... |
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The structural basis for substrate-induced changes in redox potential and spin equilibrium in cytochrome P-450CAM.
Biochemistry 28(2) , 917-22, (1989) The crystal structures of cytochrome P-450CAM complexed with the alternative substrates norcamphor and adamantanone have been refined at 2.0-A resolution and compared with the native, camphor-bound fo... |
2-Adamantanone |
MFCD00074737 |
Tricyclo[3.3.1.1(3,7)]decanone |
2-Adamantone |
2-Oxoadamantane |
adamantan-2-one |
Tricyclo(3,3,1,13,7)decanone |
Tricyclo[3.3.1.1]decan-2-on |
EINECS 211-847-2 |
4,6-Dehydroadamantanone |
adamantanone |
Tricyclo[3.3.1.1]decan-2-one |