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Home Nitros 2-nitro-1H-Indole

2-nitro-1H-Indole

CAS No.:
193686-70-3
Catalog Number:
AG00AM3O
Molecular Formula:
C8H6N2O2
Molecular Weight:
162.1454
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Product Description
Catalog Number:
AG00AM3O
Chemical Name:
2-nitro-1H-Indole
CAS Number:
193686-70-3
Molecular Formula:
C8H6N2O2
Molecular Weight:
162.1454
MDL Number:
MFCD12924639
IUPAC Name:
2-nitro-1H-indole
InChI:
InChI=1S/C8H6N2O2/c11-10(12)8-5-6-3-1-2-4-7(6)9-8/h1-5,9H
InChI Key:
HCGYMSSYSAKGPK-UHFFFAOYSA-N
SMILES:
[O-][N+](=O)c1cc2c([nH]1)cccc2
Properties
Complexity:
190  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
162.043g/mol
Formal Charge:
0
Heavy Atom Count:
12  
Hydrogen Bond Acceptor Count:
2  
Hydrogen Bond Donor Count:
1  
Isotope Atom Count:
0
Molecular Weight:
162.148g/mol
Monoisotopic Mass:
162.043g/mol
Rotatable Bond Count:
0
Topological Polar Surface Area:
61.6A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
2.6  
Literature
Title Journal
High-resolution cross-reactive array for alkaloids. Chemical communications (Cambridge, England) 20090614
Production of in vitro amplified DNA pseudolibraries and high-throughput cDNA target amplification. BMC biotechnology 20070101
Large fragment Bst DNA polymerase for whole genome amplification of DNA from formalin-fixed paraffin-embedded tissues. BMC genomics 20060101
Nitric oxide synthase inhibitors and nitric oxide donors modulate the biosynthesis of thaxtomin A, a nitrated phytotoxin produced by Streptomyces spp. Nitric oxide : biology and chemistry 20050201
Chemistry of the 2-deoxyribonolactone lesion in oligonucleotides: cleavage kinetics and products analysis. Journal of the American Chemical Society 20020807
Synthesis of nitroindole derivatives with high affinity and selectivity for melatoninergic binding sites MT(3). Journal of medicinal chemistry 20020425
Properties