Home Other Building Blocks 2-Adamantanone

2-Adamantanone

CAS No.:
700-58-3
Catalog Number:
AG00366M
Molecular Formula:
C10H14O
Molecular Weight:
150.2176
Pack Size
Purity
Availability
Location
Price(USD)
Quantity
  
5g
98%(GC)
In Stock USA
United States
$39
- +
25g
98%(GC)
In Stock USA
United States
$48
- +
100g
98%(GC)
In Stock USA
United States
$112
- +
500g
98%(GC)
In Stock USA
United States
$298
- +
Product Description
Catalog Number:
AG00366M
Chemical Name:
2-Adamantanone
CAS Number:
700-58-3
Molecular Formula:
C10H14O
Molecular Weight:
150.2176
MDL Number:
MFCD00074737
IUPAC Name:
adamantan-2-one
InChI:
InChI=1S/C10H14O/c11-10-8-2-6-1-7(4-8)5-9(10)3-6/h6-9H,1-5H2
InChI Key:
IYKFYARMMIESOX-UHFFFAOYSA-N
SMILES:
O=C1C2CC3CC1CC(C2)C3
EC Number:
211-847-2
UNII:
UI7W503L08
NSC Number:
126345
Properties
Complexity:
177  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
150.104g/mol
Formal Charge:
0
Heavy Atom Count:
11  
Hydrogen Bond Acceptor Count:
1  
Hydrogen Bond Donor Count:
0
Isotope Atom Count:
0
Molecular Weight:
150.221g/mol
Monoisotopic Mass:
150.104g/mol
Rotatable Bond Count:
0
Topological Polar Surface Area:
17.1A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
1.8  
Literature
Title Journal
Mechanically induced chemiluminescence from polymers incorporating a 1,2-dioxetane unit in the main chain. Nature chemistry 20120603
Cucurbituril adamantanediazirine complexes and consequential carbene chemistry. The Journal of organic chemistry 20120601
N'-(Adamantan-2-yl-idene)thio-phene-2-carbohydrazide. Acta crystallographica. Section E, Structure reports online 20111101
Nickel(II) complexes of tripodal 4N ligands as catalysts for alkane oxidation using m-CPBA as oxidant: ligand stereoelectronic effects on catalysis. Dalton transactions (Cambridge, England : 2003) 20111007
Spring-loading the active site of cytochrome P450cam. Metallomics : integrated biometal science 20110401
Tuning the conversion of cyclohexane into cyclohexanol/one by molecular dioxygen, protons and reducing agents at a single non-porphyrinic iron centre and chemical versatility of the tris(2-pyridylmethyl)amine TPAFe(II)Cl2 complex in mild oxidation chemistry. Dalton transactions (Cambridge, England : 2003) 20110107
Enolates in 3-D: an experimental and computational study of deprotonated 2-adamantanone. The Journal of organic chemistry 20100618
Chemoselective and biomimetic hydroxylation of hydrocarbons by non-heme micro-oxo-bridged diiron(III) catalysts using m-CPBA as oxidant. Dalton transactions (Cambridge, England : 2003) 20090714
Piperidine dispiro-1,2,4-trioxane analogues. Bioorganic & medicinal chemistry letters 20081101
2-(Tricyclo[3.3.1.1]dec-2-ylamino)ethanol hemihydrate. Acta crystallographica. Section E, Structure reports online 20080701
Novel and efficient method for the allylation of carbonyl compounds and imines using triallylaluminum. The Journal of organic chemistry 20060512
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. Journal of the American Chemical Society 20050209
Novel spiroanellated 1,2,4-trioxanes with high in vitro antimalarial activities. Bioorganic & medicinal chemistry letters 20050201
Synthesis of a silene from 1,1-dilithiosilole and 2-adamantanone. Journal of the American Chemical Society 20040505
Substrate modulates compound I formation in peroxide shunt pathway of Pseudomonas putida cytochrome P450(cam). Biochemical and biophysical research communications 20040206
6-(2-adamantan-2-ylidene-hydroxybenzoxazole)-O-sulfamate: a potent non-steroidal irreversible inhibitor of human steroid sulfatase. Bioorganic & medicinal chemistry letters 20031215
The oxidation of diamond: the geometry and stretching frequency of carbonyl on the (100) surface. Journal of the American Chemical Society 20030604
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. Chemical communications (Cambridge, England) 20030321
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. Doklady. Biochemistry and biophysics 20030101
Solid-state and solution studies of a tetrameric capsule and its guests. Angewandte Chemie (International ed. in English) 20021018
Green chemistry procedure for the synthesis of cyclic ketals from 2-adamantanone as potential cosmetic odourants. International journal of cosmetic science 20021001
Sn-zeolite beta as a heterogeneous chemoselective catalyst for Baeyer-Villiger oxidations. Nature 20010726
Effect of adamantanone derivative possessing anti-HIV properties on the redox processes in the cytochrome P-450 system. Doklady. Biochemistry and biophysics 20010101
Microbial oxidation of adamantanone by Pseudomonas putida carrying the camphor catabolic plasmid. Biochemical and biophysical research communications 19920814
Properties