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Home Aminos beta-amino-1H-indole-3-propanol

beta-amino-1H-indole-3-propanol

CAS No.:
526-53-4
Catalog Number:
AG00DOM5
Molecular Formula:
C11H14N2O
Molecular Weight:
190.2417
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Product Description
Catalog Number:
AG00DOM5
Chemical Name:
beta-amino-1H-indole-3-propanol
CAS Number:
526-53-4
Molecular Formula:
C11H14N2O
Molecular Weight:
190.2417
MDL Number:
MFCD00069710
IUPAC Name:
2-amino-3-(1H-indol-3-yl)propan-1-ol
InChI:
InChI=1S/C11H14N2O/c12-9(7-14)5-8-6-13-11-4-2-1-3-10(8)11/h1-4,6,9,13-14H,5,7,12H2
InChI Key:
UDQCRUSSQAXPJY-UHFFFAOYSA-N
SMILES:
OCC(Cc1c[nH]c2c1cccc2)N
EC Number:
208-392-7
Properties
Complexity:
186  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
190.111g/mol
Formal Charge:
0
Heavy Atom Count:
14  
Hydrogen Bond Acceptor Count:
2  
Hydrogen Bond Donor Count:
3  
Isotope Atom Count:
0
Molecular Weight:
190.246g/mol
Monoisotopic Mass:
190.111g/mol
Rotatable Bond Count:
3  
Topological Polar Surface Area:
62A^2
Undefined Atom Stereocenter Count:
1  
Undefined Bond Stereocenter Count:
0
XLogP3:
0.9  
Literature
Title Journal
Quantifying prefibrillar amyloids in vitro by using a 'thioflavin-like' spectroscopic method. Chembiochem : a European journal of chemical biology 20100903
Amino acid deprivation links BLIMP-1 to the immunomodulatory enzyme indoleamine 2,3-dioxygenase. Journal of immunology (Baltimore, Md. : 1950) 20091101
Enantioselective formal synthesis of (+)-dihydrocorynantheine and (-)-dihydrocorynantheol. The Journal of organic chemistry 20090206
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
Properties