Home Other Building Blocks 9H-Pyrido[2,3-b]indole

9H-Pyrido[2,3-b]indole

CAS No.:
244-76-8
Catalog Number:
AG002GBE
Molecular Formula:
C11H8N2
Molecular Weight:
168.1946
Pack Size
Purity
Availability
Location
Price(USD)
Quantity
  
1g
96%
In Stock USA
United States
$82
- +
5g
96%
In Stock USA
United States
$244
- +
10g
96%
In Stock USA
United States
$438
- +
25g
96%
In Stock USA
United States
$938
- +
100g
96%
In Stock USA
United States
$2625
- +
Product Description
Catalog Number:
AG002GBE
Chemical Name:
9H-Pyrido[2,3-b]indole
CAS Number:
244-76-8
Molecular Formula:
C11H8N2
Molecular Weight:
168.1946
MDL Number:
MFCD00473709
IUPAC Name:
9H-pyrido[2,3-b]indole
InChI:
InChI=1S/C11H8N2/c1-2-6-10-8(4-1)9-5-3-7-12-11(9)13-10/h1-7H,(H,12,13)
InChI Key:
BPMFPOGUJAAYHL-UHFFFAOYSA-N
SMILES:
c1ccc2c(c1)[nH]c1c2cccn1
EC Number:
205-960-6
UNII:
274Z75I9BQ
NSC Number:
67064
Properties
Complexity:
193  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
168.069g/mol
Formal Charge:
0
Heavy Atom Count:
13  
Hydrogen Bond Acceptor Count:
1  
Hydrogen Bond Donor Count:
1  
Isotope Atom Count:
0
Molecular Weight:
168.199g/mol
Monoisotopic Mass:
168.069g/mol
Rotatable Bond Count:
0
Topological Polar Surface Area:
28.7A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
2.9  
Literature
Title Journal
Discovery of 4-anilino α-carbolines as novel Brk inhibitors. Bioorganic & medicinal chemistry letters 20140415
Spectral and photophysical properties of α-carboline (1-azacarbazole) in aqueous solutions. Journal of fluorescence 20120501
A photophysical study of the α-carboline (1-azacarbazole) aggregation process. Photochemistry and photobiology 20120101
Three-component tandem reaction involving acid chlorides, terminal alkynes, and 2-aminoindole hydrochlorides: synthesis of α-carboline derivatives in aqueous conditions via regioselective [3 + 3] cyclocondensation. The Journal of organic chemistry 20111216
Electronic spectra and photophysics of the α-carboline (1-azacarbazole) monomer. Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy 20111215
Synthesis of α-carbolines via Pd-catalyzed amidation and Vilsmeier-Haack reaction of 3-acetyl-2-chloroindoles. Organic letters 20110318
Photophysics of the 6H-indolo[2,3-b]quinoline molecule: the excited-state double-proton-transfer process in perspective. The journal of physical chemistry. A 20110317
Synthesis and cytotoxicity of 1,6,8,9-substituted α-carboline derivatives. The Kaohsiung journal of medical sciences 20101101
Gamma-carboline derivatives with anti-bovine viral diarrhea virus (BVDV) activity. Bioorganic & medicinal chemistry 20080401
Photophysics of 1-azacarbazole dimers: a reappraisal. The journal of physical chemistry. A 20070913
Analysis of alpha- and beta-carbolines in mainstream smoke of reference cigarettes by gas chromatography-mass spectrometry. Journal of chromatography. A 20040813
Properties