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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
Structure of ADAMANTANONE

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

HIDE SMILES / InChI

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

PubMed

TitleDatePubMed
Microbial oxidation of adamantanone by Pseudomonas putida carrying the camphor catabolic plasmid.
1992 Aug 14
Sn-zeolite beta as a heterogeneous chemoselective catalyst for Baeyer-Villiger oxidations.
2001 Jul 26
Effect of adamantanone derivative possessing anti-HIV properties on the redox processes in the cytochrome P-450 system.
2001 May-Jun
Green chemistry procedure for the synthesis of cyclic ketals from 2-adamantanone as potential cosmetic odourants.
2002 Oct
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
Synthesis of a silene from 1,1-dilithiosilole and 2-adamantanone.
2004 May 5
Novel spiroanellated 1,2,4-trioxanes with high in vitro antimalarial activities.
2005 Feb 1
Substrate modulation of the properties and reactivity of the oxy-ferrous and hydroperoxo-ferric intermediates of cytochrome P450cam as shown by cryoreduction-EPR/ENDOR spectroscopy.
2005 Feb 9
Novel and efficient method for the allylation of carbonyl compounds and imines using triallylaluminum.
2006 May 12
2-(Tricyclo[3.3.1.1]dec-2-ylamino)ethanol hemihydrate.
2008 Jun 7
Piperidine dispiro-1,2,4-trioxane analogues.
2008 Nov 1
Chemoselective and biomimetic hydroxylation of hydrocarbons by non-heme micro-oxo-bridged diiron(III) catalysts using m-CPBA as oxidant.
2009 Jul 14
Enolates in 3-D: an experimental and computational study of deprotonated 2-adamantanone.
2010 Jun 18
Patents
Substance Class Chemical
Created
by admin
on Sat Dec 16 09:05:57 GMT 2023
Edited
by admin
on Sat Dec 16 09:05:57 GMT 2023
Record UNII
UI7W503L08
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
ADAMANTANONE
Systematic Name English
NSC-126345
Code English
TRICYCLO(3.3.1.13,7)DECAN-2-ONE
Systematic Name English
2-OXOADAMANTANE
Systematic Name English
2-ADAMANTANONE
Systematic Name English
2-ADAMANTONE
Common Name English
Code System Code Type Description
FDA UNII
UI7W503L08
Created by admin on Sat Dec 16 09:05:57 GMT 2023 , Edited by admin on Sat Dec 16 09:05:57 GMT 2023
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CAS
700-58-3
Created by admin on Sat Dec 16 09:05:57 GMT 2023 , Edited by admin on Sat Dec 16 09:05:57 GMT 2023
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EPA CompTox
DTXSID9022108
Created by admin on Sat Dec 16 09:05:57 GMT 2023 , Edited by admin on Sat Dec 16 09:05:57 GMT 2023
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CHEBI
40611
Created by admin on Sat Dec 16 09:05:57 GMT 2023 , Edited by admin on Sat Dec 16 09:05:57 GMT 2023
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PUBCHEM
64151
Created by admin on Sat Dec 16 09:05:57 GMT 2023 , Edited by admin on Sat Dec 16 09:05:57 GMT 2023
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DRUG BANK
DB02125
Created by admin on Sat Dec 16 09:05:57 GMT 2023 , Edited by admin on Sat Dec 16 09:05:57 GMT 2023
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NSC
126345
Created by admin on Sat Dec 16 09:05:57 GMT 2023 , Edited by admin on Sat Dec 16 09:05:57 GMT 2023
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ECHA (EC/EINECS)
211-847-2
Created by admin on Sat Dec 16 09:05:57 GMT 2023 , Edited by admin on Sat Dec 16 09:05:57 GMT 2023
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WIKIPEDIA
Adamantanone
Created by admin on Sat Dec 16 09:05:57 GMT 2023 , Edited by admin on Sat Dec 16 09:05:57 GMT 2023
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