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Home Other Building Blocks 5-Hydroxy-2-adamantanone

5-Hydroxy-2-adamantanone

CAS No.:
20098-14-0
Catalog Number:
AG002D4I
Molecular Formula:
C10H14O2
Molecular Weight:
166.2170
Pack Size
Purity
Availability
Location
Price(USD)
Quantity
  
1g
99%(GC)
In Stock USA
United States
$37
- +
5g
99%(GC)
In Stock USA
United States
$55
- +
25g
99%(GC)
In Stock USA
United States
$154
- +
50g
95%
In Stock USA
United States
$188
- +
500g
99%(GC)
In Stock USA
United States
$865
- +
Product Description
Catalog Number:
AG002D4I
Chemical Name:
5-Hydroxy-2-adamantanone
CAS Number:
20098-14-0
Molecular Formula:
C10H14O2
Molecular Weight:
166.2170
MDL Number:
MFCD00192211
IUPAC Name:
5-hydroxyadamantan-2-one
InChI:
InChI=1S/C10H14O2/c11-9-7-1-6-2-8(9)5-10(12,3-6)4-7/h6-8,12H,1-5H2
InChI Key:
TZBDEVBNMSLVKT-UHFFFAOYSA-N
SMILES:
O=C1C2CC3CC1CC(C2)(C3)O
UNII:
7J4759Y5J1
NSC Number:
760375
Properties
Complexity:
228  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
166.099g/mol
Formal Charge:
0
Heavy Atom Count:
12  
Hydrogen Bond Acceptor Count:
2  
Hydrogen Bond Donor Count:
1  
Isotope Atom Count:
0
Molecular Weight:
166.22g/mol
Monoisotopic Mass:
166.099g/mol
Rotatable Bond Count:
0
Topological Polar Surface Area:
37.3A^2
Undefined Atom Stereocenter Count:
2  
Undefined Bond Stereocenter Count:
0
XLogP3:
0.5  
Literature
Title Journal
[Adamantane derivate enhances cerebral blood flow under conditions of ischemic brain damage]. Eksperimental'naia i klinicheskaia farmakologiia 20120101
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