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271-29-4 | 1H-Pyrrolo[2,3-c]pyridine
CAS No: 271-29-4 Catalog No: AG003N33 MDL No:MFCD01686899
Product Description
Catalog Number:
AG003N33
Chemical Name:
1H-Pyrrolo[2,3-c]pyridine
CAS Number:
271-29-4
Molecular Formula:
C7H6N2
Molecular Weight:
118.1359
MDL Number:
MFCD01686899
IUPAC Name:
1H-pyrrolo[2,3-c]pyridine
InChI:
InChI=1S/C7H6N2/c1-3-8-5-7-6(1)2-4-9-7/h1-5,9H
InChI Key:
XLKDJOPOOHHZAN-UHFFFAOYSA-N
SMILES:
c1ncc2c(c1)cc[nH]2
Properties
Complexity:
103
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
118.053g/mol
Formal Charge:
0
Heavy Atom Count:
9
Hydrogen Bond Acceptor Count:
1
Hydrogen Bond Donor Count:
1
Isotope Atom Count:
0
Molecular Weight:
118.139g/mol
Monoisotopic Mass:
118.053g/mol
Rotatable Bond Count:
0
Topological Polar Surface Area:
28.7A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
1
Literature
| Title | Journal |
|---|---|
| Synthesis of 2,5-disubstituted 6-azaindoles from substituted aziridines via intramolecular cyclization. | Organic letters 20120615 |
| Structure-based optimization of potent 4- and 6-azaindole-3-carboxamides as renin inhibitors. | Bioorganic & medicinal chemistry letters 20110915 |
| Synthesis of azaheterocycles from aryl ketone O-acetyl oximes and internal alkynes by Cu-Rh bimetallic relay catalysts. | The Journal of organic chemistry 20110805 |
| Access to pyrrolo-pyridines by gold-catalyzed hydroarylation of pyrroles tethered to terminal alkynes. | Beilstein journal of organic chemistry 20110101 |
| Novel 1H-pyrrolo[2,3-c]pyridines as acid pump antagonists (APAs). | Bioorganic & medicinal chemistry letters 20100901 |
| Evaluation of basic, heterocyclic ring systems as templates for use as potassium competitive acid blockers (pCABs). | Bioorganic & medicinal chemistry letters 20091201 |
| Synthesis of 4- and 6-azaindoles via the Fischer reaction. | Organic letters 20091119 |
| Discovery of 1-[4-(3-chlorophenylamino)-1-methyl-1H-pyrrolo[3,2-c]pyridin-7-yl]-1-morpholin-4-ylmethanone (GSK554418A), a brain penetrant 5-azaindole CB2 agonist for the treatment of chronic pain. | Journal of medicinal chemistry 20091008 |
| Design, synthesis and dopamine D4 receptor binding activities of new N-heteroaromatic 5/6-ring Mannich bases. | Bioorganic & medicinal chemistry 20090701 |
| Magnetic interactions in two heterobridged dinuclear copper(II) complexes: orbital complementarity or countercomplementarity? | The journal of physical chemistry. A 20080911 |
| Solvent-dependent oxidations of 5- and 6-azaindoles to trioxopyrrolopyridines and functionalised azaindoles. | Organic & biomolecular chemistry 20080421 |
| A novel one-step synthesis of 2-substituted 6-azaindoles from 3-amino-4-picoline and carboxylic esters. | The Journal of organic chemistry 20050805 |
| Novel potent 5-HT(1F) receptor agonists: structure-activity studies of a series of substituted N-[3-(1-methyl-4-piperidinyl)-1H-pyrrolo[3,2-b]pyridin-5-yl]amides. | Journal of medicinal chemistry 20030703 |
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