700-57-2 | 2-Adamantanol

Packsize	Purity	Availability	Price	Discounted Price
1g	95%	in stock	$14.00	$10.00
5g	95%	in stock	$15.00	$10.00
25g	95%	in stock	$48.00	$33.00
100g	95%	in stock	$162.00	$113.00

Description

• Catalog Number: AB60926
• Chemical Name: 2-Adamantanol
• CAS Number: 700-57-2
• Molecular Formula: C10H16O
• Molecular Weight: 152.2334
• MDL Number: MFCD00074744
• SMILES: OC1C2CC3CC1CC(C2)C3
• NSC Number: 193480

Computed Properties

• Complexity: 148
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 11
• Hydrogen Bond Acceptor Count: 1
• Hydrogen Bond Donor Count: 1
• XLogP3: 1.9

Literature

• 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