3182-95-4 | L-Phenylalaninol

Packsize	Purity	Availability	Price	Discounted Price
5g	99%	in stock	$12.00	$8.00
10g	99%	in stock	$15.00	$10.00
25g	95%	in stock	$17.00	$12.00
100g	95%	in stock	$21.00	$15.00
500g	95%	in stock	$104.00	$73.00

Description

• Catalog Number: AB46391
• Chemical Name: L-Phenylalaninol
• CAS Number: 3182-95-4
• Molecular Formula: C9H13NO
• Molecular Weight: 151.2056
• MDL Number: MFCD00004732
• SMILES: OC[C@H](Cc1ccccc1)N

Computed Properties

• Complexity: 99.7
• Covalently-Bonded Unit Count: 1
• Defined Atom Stereocenter Count: 1
• Heavy Atom Count: 11
• Hydrogen Bond Acceptor Count: 2
• Hydrogen Bond Donor Count: 2
• Rotatable Bond Count: 3
• XLogP3: 0.7

Literature

• 20-Residue and 11-residue peptaibols from the fungus Trichoderma longibrachiatum are synergistic in forming Na+/K+ -permeable channels and adverse action towards mammalian cells.

  The FEBS journal 20121101

• A colorimetric chiral sensor based on chiral crown ether for the recognition of the two enantiomers of primary amino alcohols and amines.

  Chirality 20110401

• A Standard Protocol for the Calibration of Capillary Electrophoresis (CE) Equipment.

  Scientia pharmaceutica 20110101

• Absolute configurations and CD spectra of axially chiral biphenyls prepared in a facile manner by crystallization-induced configuration transformation.

  Chirality 20100801

• Synthesis of enantiopure 2-aryl-2-methoxypropionic acids and determination of their absolute configurations by X-ray crystallography.

  Chirality 20080301

• Direct high-performance liquid chromatographic separation of the enantiomers of an aromatic amine and four aminoalcohols using polysaccharide chiral stationary phases and acidic additive.

  Chirality 20070801

• Straightforward methodology for the enantioselective synthesis of benzo[a]- and indolo[2,3-a]quinolizidines.

  The Journal of organic chemistry 20070706

• New route to enantiopure MalphaNP acid, a powerful resolution and chiral 1H NMR anisotropy reagent.

  Chirality 20070515

• Microsphere-based protease assays and screening application for lethal factor and factor Xa.

  Cytometry. Part A : the journal of the International Society for Analytical Cytology 20060501

• Synthesis and activity of 2-oxoamides containing long chain beta-amino acids.

  Journal of peptide science : an official publication of the European Peptide Society 20050701

• Chiral oxime ethers in asymmetric synthesis. O-(1-Phenylbutyl)benzyloxyacetaldoxime, a versatile reagent for the asymmetric synthesis of protected 1,2-aminoalcohols, alpha-amino acid derivatives, and 2-hydroxymethyl nitrogen heterocycles including iminosugars.

  Organic & biomolecular chemistry 20050407

• Chiral bis(amino alcohol)oxalamide gelators-gelation properties and supramolecular organization: racemate versus pure enantiomer gelation.

  Chemistry (Weinheim an der Bergstrasse, Germany) 20031121

• Identification of a novel system L amino acid transporter structurally distinct from heterodimeric amino acid transporters.

  The Journal of biological chemistry 20031031

• Resolution of 1- and 2-naphthylmethoxyacetic acids, NMR reagents for absolute configuration determination, by use of L-phenylalaninol.

  Chirality 20030801

• Tuning and enhancing enantioselective quenching of calixarene hosts by chiral guest amines.

  Analytical chemistry 20020101

• Enantioselective molecular sensing of aromatic amines using tetra-(S)-di-2-naphthylprolinol calix[4]arene.

  The Analyst 20010701

• Chemotactic peptide analogues. Synthesis and chemotactic activity of N-formyl-Met-Leu-Phe analogues containing (S)-phenylalaninol derivatives.

  Archiv der Pharmazie 19950901