Details
Stereochemistry | ACHIRAL |
Molecular Formula | C10H14O |
Molecular Weight | 150.2176 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
O=C1C2CC3CC(C2)CC1C3
InChI
InChIKey=IYKFYARMMIESOX-UHFFFAOYSA-N
InChI=1S/C10H14O/c11-10-8-2-6-1-7(4-8)5-9(10)3-6/h6-9H,1-5H2
Molecular Formula | C10H14O |
Molecular Weight | 150.2176 |
Charge | 0 |
Count |
|
Stereochemistry | ACHIRAL |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Optical Activity | NONE |
Approval Year
PubMed
Title | Date | PubMed |
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Effect of adamantanone derivative possessing anti-HIV properties on the redox processes in the cytochrome P-450 system. | 2001 May-Jun |
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Green chemistry procedure for the synthesis of cyclic ketals from 2-adamantanone as potential cosmetic odourants. | 2002 Oct |
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Solid-state and solution studies of a tetrameric capsule and its guests. | 2002 Oct 18 |
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6-(2-adamantan-2-ylidene-hydroxybenzoxazole)-O-sulfamate: a potent non-steroidal irreversible inhibitor of human steroid sulfatase. | 2003 Dec 15 |
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An adamantanone derivative that is an original modulator of redox processes in the cytochrome P-450 system can serve as an effective remedy against obliterating angiopathy of lower extremities. | 2003 Jul-Aug |
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The oxidation of diamond: the geometry and stretching frequency of carbonyl on the (100) surface. | 2003 Jun 4 |
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Reversible C-C bond formation: solid state structure of the aldol-like addition product of adamantanone to a 1,5-diazapentadienyllithium, and its solution state retro-aldol dissociation. | 2003 Mar 21 |
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Novel and efficient method for the allylation of carbonyl compounds and imines using triallylaluminum. | 2006 May 12 |
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2-(Tricyclo[3.3.1.1]dec-2-ylamino)ethanol hemihydrate. | 2008 Jun 7 |
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Piperidine dispiro-1,2,4-trioxane analogues. | 2008 Nov 1 |
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Chemoselective and biomimetic hydroxylation of hydrocarbons by non-heme micro-oxo-bridged diiron(III) catalysts using m-CPBA as oxidant. | 2009 Jul 14 |
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Enolates in 3-D: an experimental and computational study of deprotonated 2-adamantanone. | 2010 Jun 18 |
Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 09:05:57 GMT 2023
by
admin
on
Sat Dec 16 09:05:57 GMT 2023
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Record UNII |
UI7W503L08
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Record Status |
Validated (UNII)
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Record Version |
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Adamantanone
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