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13228-40-5

13228-40-5 | 1H-Indole, 2-(2-pyridinyl)-

CAS No: 13228-40-5 Catalog No: AG0010HJ MDL No:MFCD00033466

Product Description

Catalog Number:
AG0010HJ
Chemical Name:
1H-Indole, 2-(2-pyridinyl)-
CAS Number:
13228-40-5
Molecular Formula:
C13H10N2
Molecular Weight:
194.2319
MDL Number:
MFCD00033466
IUPAC Name:
2-pyridin-2-yl-1H-indole
InChI:
InChI=1S/C13H10N2/c1-2-6-11-10(5-1)9-13(15-11)12-7-3-4-8-14-12/h1-9,15H
InChI Key:
OLGGLCIDAMICTA-UHFFFAOYSA-N
SMILES:
c1ccc(nc1)c1cc2c([nH]1)cccc2
NSC Number:
112668

Properties

Complexity:
217  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
194.084g/mol
Formal Charge:
0
Heavy Atom Count:
15  
Hydrogen Bond Acceptor Count:
1  
Hydrogen Bond Donor Count:
1  
Isotope Atom Count:
0
Molecular Weight:
194.237g/mol
Monoisotopic Mass:
194.084g/mol
Rotatable Bond Count:
1  
Topological Polar Surface Area:
28.7A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
3.3  

Literature

Title Journal
Neutral cuprous complexes as ratiometric oxygen gas sensors. Dalton transactions (Cambridge, England : 2003) 20120128
Steric and electronic influence on photochromic switching of N,C-chelate four-coordinate organoboron compounds. Chemistry (Weinheim an der Bergstrasse, Germany) 20100426
Isocyanate-, isothiocyanate-, urea-, and thiourea-substituted boron dipyrromethene dyes as fluorescent probes. The Journal of organic chemistry 20060414
2-Pyridin-2-yl-1H-indole derivatives: synthesis, estrogen receptor binding affinity, and photophysical properties. Bioorganic chemistry 20060201
Parallel synthesis of 5-cyano-6-aryl-2-thiouracil derivatives as inhibitors for hepatitis C viral NS5B RNA-dependent RNA polymerase. Bioorganic chemistry 20060201

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