Home Aminos Benzenepropanol, β-amino-

Benzenepropanol, β-amino-

CAS No.:
16088-07-6
Catalog Number:
AG001VFU
Molecular Formula:
C9H13NO
Molecular Weight:
151.2056
Pack Size
Purity
Availability
Location
Price(USD)
Quantity
  
1g
95%
In Stock USA
United States
$73
- +
5g
95%
In Stock USA
United States
$182
- +
25g
95%
In Stock USA
United States
$508
- +
Product Description
Catalog Number:
AG001VFU
Chemical Name:
Benzenepropanol, β-amino-
CAS Number:
16088-07-6
Molecular Formula:
C9H13NO
Molecular Weight:
151.2056
MDL Number:
MFCD00066689
IUPAC Name:
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
InChI Key:
STVVMTBJNDTZBF-UHFFFAOYSA-N
SMILES:
OCC(Cc1ccccc1)N
Properties
Complexity:
99.7  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
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:
1  
Undefined Bond Stereocenter Count:
0
XLogP3:
0.7  
Literature
Title Journal
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
Properties