Home Other Building Blocks 2-Adamantanol

2-Adamantanol

CAS No.:
700-57-2
Catalog Number:
AG003GBQ
Molecular Formula:
C10H16O
Molecular Weight:
152.2334
Pack Size
Purity
Availability
Location
Price(USD)
Quantity
  
1g
95%
In Stock USA
United States
$33
- +
5g
95%
In Stock USA
United States
$54
- +
25g
95%
In Stock USA
United States
$110
- +
100g
95%
In Stock USA
United States
$325
- +
Product Description
Catalog Number:
AG003GBQ
Chemical Name:
2-Adamantanol
CAS Number:
700-57-2
Molecular Formula:
C10H16O
Molecular Weight:
152.2334
MDL Number:
MFCD00074744
IUPAC Name:
adamantan-2-ol
InChI:
InChI=1S/C10H16O/c11-10-8-2-6-1-7(4-8)5-9(10)3-6/h6-11H,1-5H2
InChI Key:
FOWDOWQYRZXQDP-UHFFFAOYSA-N
SMILES:
OC1C2CC3CC1CC(C2)C3
EC Number:
211-846-7
NSC Number:
193480
Properties
Complexity:
148  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
152.12g/mol
Formal Charge:
0
Heavy Atom Count:
11  
Hydrogen Bond Acceptor Count:
1  
Hydrogen Bond Donor Count:
1  
Isotope Atom Count:
0
Molecular Weight:
152.237g/mol
Monoisotopic Mass:
152.12g/mol
Rotatable Bond Count:
0
Topological Polar Surface Area:
20.2A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
1.9  
Literature
Title Journal
Sterically congested quinone methides in photodehydration reactions of 4-hydroxybiphenyl derivatives and investigation of their antiproliferative activity. Photochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology 20111201
Discovery and optimization of adamantyl carbamate inhibitors of 11β-HSD1. Bioorganic & medicinal chemistry letters 20101115
Synthesis and SAR studies of 1,4-benzoxazine MenB inhibitors: novel antibacterial agents against Mycobacterium tuberculosis. Bioorganic & medicinal chemistry letters 20101101
Bioconversion of 1-adamantanol to 1,3-adamantanediol using Streptomyces sp. SA8 oxidation system. Journal of bioscience and bioengineering 20100601
Photochemical formation and chemistry of long-lived adamantylidene-quinone methides and 2-adamantyl cations. The Journal of organic chemistry 20100101
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
OH-stretching red shifts in bulky hydrogen-bonded alcohols: jet spectroscopy and modeling. The journal of physical chemistry. A 20060817
Regioselective hydroxylation of adamantane by Streptomyces griseoplanus cells. Applied microbiology and biotechnology 20060701
Discovery and preclinical profile of Saxagliptin (BMS-477118): a highly potent, long-acting, orally active dipeptidyl peptidase IV inhibitor for the treatment of type 2 diabetes. Journal of medicinal chemistry 20050728
Low-temperature X-ray structural studies of the ester and ether derivatives of cis- and trans-4-tert-butyl cyclohexanol and 2-adamantanol: application of the variable oxygen probe to determine the relative sigma-donor ability of C-H and C-C bonds. Organic & biomolecular chemistry 20030907
A theoretical study of reactivity and regioselectivity in the hydroxylation of adamantane by ferrate(VI). The Journal of organic chemistry 20030516
Synthesis and antimicrobial activity of new adamantane derivatives III. Farmaco (Societa chimica italiana : 1989) 20020801
Properties