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21109-25-1

21109-25-1 | 1H-Indole-2-methanamine

CAS No: 21109-25-1 Catalog No: AG002L5P MDL No:MFCD03422512

Product Description

Catalog Number:
AG002L5P
Chemical Name:
1H-Indole-2-methanamine
CAS Number:
21109-25-1
Molecular Formula:
C9H10N2
Molecular Weight:
146.1891
MDL Number:
MFCD03422512
IUPAC Name:
1H-indol-2-ylmethanamine
InChI:
InChI=1S/C9H10N2/c10-6-8-5-7-3-1-2-4-9(7)11-8/h1-5,11H,6,10H2
InChI Key:
RNAODKZCUVVPEN-UHFFFAOYSA-N
SMILES:
NCc1cc2c([nH]1)cccc2

Properties

Complexity:
136  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
146.084g/mol
Formal Charge:
0
Heavy Atom Count:
11  
Hydrogen Bond Acceptor Count:
1  
Hydrogen Bond Donor Count:
2  
Isotope Atom Count:
0
Molecular Weight:
146.193g/mol
Monoisotopic Mass:
146.084g/mol
Rotatable Bond Count:
1  
Topological Polar Surface Area:
41.8A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
1  

Literature

Title Journal
Metabolism and metabolites of dithiocarbamates in the plant pathogenic fungus Leptosphaeria maculans. Journal of agricultural and food chemistry 20120815
Evaluation of novel aminomethyl indole derivatives as Src kinase inhibitors and antioxidant agents. Chemotherapy 20110101
Construction of indole- and isoquinoline-fused nitrogen-containing heterocycles through copper-catalyzed multi-component reaction. Yakugaku zasshi : Journal of the Pharmaceutical Society of Japan 20100701
Investigation of aminomethyl indole derivatives as hyaluronidase inhibitors. Zeitschrift fur Naturforschung. C, Journal of biosciences 20100101
Novel aminomethylindole derivatives as inhibitors of pp60c-Src tyrosine kinase: synthesis and biological activity. Chemical biology & drug design 20081201
Highly enantioselective friedel-crafts reaction of 4,7-dihydroindoles with imines by chiral phosphoric acids: facile access to 2-indolyl methanamine derivatives. Chemistry (Weinheim an der Bergstrasse, Germany) 20080101

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