ADAMANTANONE

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 Search

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

Title	Date	PubMed
Enolates in 3-D: an experimental and computational study of deprotonated 2-adamantanone.	2010-06-18	20496940
Chemoselective and biomimetic hydroxylation of hydrocarbons by non-heme micro-oxo-bridged diiron(III) catalysts using m-CPBA as oxidant.	2009-07-14	19562169
Piperidine dispiro-1,2,4-trioxane analogues.	2008-11-01	18845438
2-(Tricyclo[3.3.1.1]dec-2-ylamino)ethanol hemihydrate.	2008-06-07	21202865
Novel and efficient method for the allylation of carbonyl compounds and imines using triallylaluminum.	2006-05-12	16674079
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.	2005-02-09	15686372
Novel spiroanellated 1,2,4-trioxanes with high in vitro antimalarial activities.	2005-02-01	15664819
Synthesis of a silene from 1,1-dilithiosilole and 2-adamantanone.	2004-05-05	15113186
Substrate modulates compound I formation in peroxide shunt pathway of Pseudomonas putida cytochrome P450(cam).	2004-02-06	14733951
6-(2-adamantan-2-ylidene-hydroxybenzoxazole)-O-sulfamate: a potent non-steroidal irreversible inhibitor of human steroid sulfatase.	2003-12-15	14643316
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.	2003-10-09	14531067
The oxidation of diamond: the geometry and stretching frequency of carbonyl on the (100) surface.	2003-06-04	12769547
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.	2003-03-21	12703802
Solid-state and solution studies of a tetrameric capsule and its guests.	2002-10-18	12386850
Green chemistry procedure for the synthesis of cyclic ketals from 2-adamantanone as potential cosmetic odourants.	2002-10	18498518
Effect of adamantanone derivative possessing anti-HIV properties on the redox processes in the cytochrome P-450 system.	2001-11-20	11712183
Sn-zeolite beta as a heterogeneous chemoselective catalyst for Baeyer-Villiger oxidations.	2001-07-26	11473313
Microbial oxidation of adamantanone by Pseudomonas putida carrying the camphor catabolic plasmid.	1992-08-14	1510672

Patents

Substance Class	Chemical Created by `admin` on `Mon Mar 31 22:29:35 GMT 2025` Edited by `admin` on `Mon Mar 31 22:29:35 GMT 2025`
Record UNII	UI7W503L08
Record Status	`Validated (UNII)`
Record Version

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Name

Type

Language

NSC-126345

Preferred Name

English

ADAMANTANONE

Systematic Name

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