Home Other Building Blocks L-Phenylalaninol

L-Phenylalaninol

CAS No.:
3182-95-4
Catalog Number:
AG00353Z
Molecular Formula:
C9H13NO
Molecular Weight:
151.2056
Pack Size
Purity
Availability
Location
Price(USD)
Quantity
  
5g
98%
In Stock USA
United States
$13
- +
10g
95%
In Stock USA
United States
$14
- +
25g
98%
In Stock USA
United States
$30
- +
100g
98%
In Stock USA
United States
$88
- +
500g
98%
In Stock USA
United States
$350
- +
Product Description
Catalog Number:
AG00353Z
Chemical Name:
L-Phenylalaninol
CAS Number:
3182-95-4
Molecular Formula:
C9H13NO
Molecular Weight:
151.2056
MDL Number:
MFCD00004732
IUPAC Name:
(2S)-2-amino-3-phenylpropan-1-ol
InChI:
InChI=1S/C9H13NO/c10-9(7-11)6-8-4-2-1-3-5-8/h1-5,9,11H,6-7,10H2/t9-/m0/s1
InChI Key:
STVVMTBJNDTZBF-VIFPVBQESA-N
SMILES:
OC[C@H](Cc1ccccc1)N
EC Number:
221-674-4
UNII:
9GE9QOP0ET
Properties
Complexity:
99.7  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
1  
Defined Bond Stereocenter Count:
0
Exact Mass:
151.1g/mol
Formal Charge:
0
Heavy Atom Count:
11  
Hydrogen Bond Acceptor Count:
2  
Hydrogen Bond Donor Count:
2  
Isotope Atom Count:
0
Molecular Weight:
151.209g/mol
Monoisotopic Mass:
151.1g/mol
Rotatable Bond Count:
3  
Topological Polar Surface Area:
46.2A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
0.7  
Literature
Title Journal
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
Properties