16088-07-6 | Benzenepropanol, β-amino-

Packsize	Purity	Availability	Price	Discounted Price
5g	97%	in stock	$16.00	$11.00
100g	95%	in stock	$243.00	$170.00
500g	95%	in stock	$1,094.00	$766.00

Description

• Catalog Number: AA87202
• Chemical Name: Benzenepropanol, β-amino-
• CAS Number: 16088-07-6
• Molecular Formula: C9H13NO
• Molecular Weight: 151.2056
• MDL Number: MFCD00066689
• SMILES: OCC(Cc1ccccc1)N

Computed Properties

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

Literature

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

  Chirality 20110401

• Synthesis and SAR studies of 1,4-benzoxazine MenB inhibitors: novel antibacterial agents against Mycobacterium tuberculosis.

  Bioorganic & medicinal chemistry letters 20101101

• 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

• 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

• Cytotoxicity of enantiomers of gossypol Schiff's bases and optical stability of gossypolone.

  European journal of medicinal chemistry 20040701

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

  Chemistry (Weinheim an der Bergstrasse, Germany) 20031121

• Peptide inhibitors of CDK2-cyclin A that target the cyclin recruitment-site: structural variants of the C-terminal Phe.

  Bioorganic & medicinal chemistry letters 20020916

• Optically active BINOL core-based phenyleneethynylene dendrimers for the enantioselective fluorescent recognition of amino alcohols.

  The Journal of organic chemistry 20010907

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

  Archiv der Pharmazie 19950901