6351-10-6 | 1-Indanol

Packsize	Purity	Availability	Price	Discounted Price
5g	98%	in stock	$12.00	$8.00
10g	98%	in stock	$18.00	$12.00
25g	98%	in stock	$29.00	$20.00
100g	98%	in stock	$86.00	$60.00
500g	98%	in stock	$356.00	$249.00

Description

• Catalog Number: AB58460
• Chemical Name: 1-Indanol
• CAS Number: 6351-10-6
• Molecular Formula: C9H10O
• Molecular Weight: 134.17510000000001
• MDL Number: MFCD00004009
• SMILES: OC1CCc2c1cccc2
• NSC Number: 31258

Computed Properties

• Complexity: 122
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 10
• Hydrogen Bond Acceptor Count: 1
• Hydrogen Bond Donor Count: 1
• Undefined Atom Stereocenter Count: 2
• XLogP3: 1.5

Literature

• Synthesis and biological evaluation of novel homochiral carbocyclic nucleosides from 1-amino-2-indanols.

  Bioorganic & medicinal chemistry 20121001

• Synthesis, X-ray analysis, and biological evaluation of a new class of stereopure lactam-based HIV-1 protease inhibitors.

  Journal of medicinal chemistry 20120322

• Gold nanoparticles incarcerated in nanoporous syndiotactic polystyrene matrices as new and efficient catalysts for alcohol oxidations.

  Chemistry (Weinheim an der Bergstrasse, Germany) 20120109

• Structural features determining the intestinal epithelial permeability and efflux of novel HIV-1 protease inhibitors.

  Journal of pharmaceutical sciences 20110901

• Efficient catalytic cycloalkane oxidation employing a 'helmet' phthalocyaninato iron(III) complex.

  Dalton transactions (Cambridge, England : 2003) 20110614

• Synthesis and evaluation of indatraline-based inhibitors for trypanothione reductase.

  ChemMedChem 20110207

• Rhodium(I)-catalyzed 1,4-silicon shift of unactivated silanes from aryl to alkyl: enantioselective synthesis of indanol derivatives.

  Angewandte Chemie (International ed. in English) 20101227

• Naturally occurring variants of human aldo-keto reductases with reduced in vitro metabolism of daunorubicin and doxorubicin.

  The Journal of pharmacology and experimental therapeutics 20101201

• Characterization of a rat NADPH-dependent aldo-keto reductase (AKR1B13) induced by oxidative stress.

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• Role of human aldo-keto-reductase AKR1B10 in the protection against toxic aldehydes.

  Chemico-biological interactions 20090316

• Fluorescence spectroscopy of jet-cooled chiral (+/-)-indan-1-ol and its cluster with (+/-)-methyl- and ethyl-lactate.

  The Journal of chemical physics 20061107

• An expedited approach to the vitamin D trans-hydrindane building block from the Hajos dione.

  Organic letters 20060608

• Conformational landscapes and free-jet rotational spectrum of indan-1-ol.

  Chemphyschem : a European journal of chemical physics and physical chemistry 20060313

• Electronic effects of ring substituents on triplet benzylic biradicals.

  Organic letters 20060216

• Enzymatic properties of a member (AKR1C19) of the aldo-keto reductase family.

  Biological & pharmaceutical bulletin 20050601

• Evaluation of (+)-sparteine-like diamines for asymmetric synthesis.

  The Journal of organic chemistry 20040820

• Unexpectedly small ortho-oxygen substituent effects on stabilities of benzylic carbocations.

  Journal of the American Chemical Society 20040818

• Degradation of aromatic hydrocarbons by Sphingomonas paucimobilis strain EPA505.

  Archives of environmental contamination and toxicology 20040801

• Heterogeneous adsorption of 1-indanol on cellulose tribenzoate and adsorption energy distribution of the two enantiomers.

  Analytical chemistry 20040101

• Modeling of the separation of two enantiomers using a microbore column.

  Journal of chromatography. A 20031212

• Comparison of the binary equilibrium isotherms of the 1-indanol enantiomers on three high-performance liquid chromatography columns of different sizes.

  Journal of chromatography. A 20031010

• Oxidative kinetic resolution of racemic alcohols catalyzed by chiral ferrocenyloxazolinylphosphine-ruthenium complexes.

  The Journal of organic chemistry 20030725

• Determination of the single component and competitive adsorption isotherms of the 1-indanol enantiomers by the inverse method.

  Journal of chromatography. A 20030711

• Equivalent models of indanol isomers adsorption on cellulose tribenzoate.

  Biotechnology progress 20030101

• Improvement in the selectivity and metabolic stability of the serotonin 5-HT(1A) ligand, S 15535: a series of cis- and trans-2-(arylcycloalkylamine) 1-indanols.

  Journal of medicinal chemistry 20020103

• Synthesis of enantiopure oxorhenium(V) and arylimidorhenium(V) '3 + 2' Schiff base complexes. X-ray diffraction, cyclic voltammetry, UV-vis, and circular dichroism characterizations.

  Inorganic chemistry 20011217

• Enantioselective routes to both enantiomers of aryl alcohols with a single catalyst antipode: Ru and Os transfer hydrogenation catalysts.

  Organic letters 20011115

• Expression and kinetic properties of a recombinant 3 alpha-hydroxysteroid/dihydrodiol dehydrogenase isoenzyme of human liver.

  Journal of biochemistry 19950801