5-Azaindole - CAS 271-34-1

Catalog:	BB019478
Product Name:	5-Azaindole
CAS:	271-34-1
Synonyms:	1H-pyrrolo[3,2-c]pyridine; 1H-pyrrolo[3,2-c]pyridine

Technical Data

Safety and Hazards

Patents

Literatures

Computed Properties

IUPAC Name:	1H-pyrrolo[3,2-c]pyridine
Description:	5-Azaindole was used as a reactant in preparation of site-selective azaindole arylation at the azine and azole rings via N-oxide activation.
Molecular Weight:	118.14
Molecular Formula:	C7H6N2
Canonical SMILES:	C1=CNC2=C1C=NC=C2
InChI:	InChI=1S/C7H6N2/c1-4-9-7-2-3-8-5-6(1)7/h1-5,9H
InChI Key:	SRSKXJVMVSSSHB-UHFFFAOYSA-N
Boiling Point:	295.8 °C at 760 mmHg
Density:	1.242 g/cm³
MDL:	MFCD00955936
LogP:	1.56290

Publication Number	Title	Priority Date
CN-113429427-A	Heterocyclic compounds, process for their preparation and their use as pharmaceuticals	20210705
CN-111978320-A	Synthesis method of 1H-pyrrolo [3, 2-c ] pyridine-6-alcohol	20200915
WO-2021209765-A2	Methods and products	20200417
CN-111196778-A	Synthetic method of 3-ethylamino pyrrole compound	20200114
WO-2021127333-A1	Trpml modulators	20191219

PMID	Publication Date	Title	Journal
28340368	20170505	Synthesis, molecular docking, antimycobacterial and antimicrobial evaluation of new pyrrolo[3,2-c]pyridine Mannich bases	European journal of medicinal chemistry
22898254	20120915	Discovery of the investigational drug TAK-441, a pyrrolo[3,2-c]pyridine derivative, as a highly potent and orally active hedgehog signaling inhibitor: modification of the core skeleton for improved solubility	Bioorganic & medicinal chemistry
22647720	20120701	Design, synthesis, and antiproliferative activity of new 1H-pyrrolo[3,2-c]pyridine derivatives against melanoma cell lines. Part 2	Bioorganic & medicinal chemistry letters
22587741	20120601	Palladium-catalyzed synthesis of 2,3-disubstituted 5-azaindoles via heteroannulation reaction and of 2-substituted 5-azaindoles through domino sila-Sonogashira/5-endo cyclization	The Journal of organic chemistry
22335894	20120301	New aromatase inhibitors from the 3-pyridyl arylether and 1-aryl pyrrolo[2,3-c]pyridine series	Bioorganic & medicinal chemistry letters

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Related Functional Groups

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[1021339-19-4]
6-Chloro-4-azaindole

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GHS Hazard Statement:	H315 (100%): Causes skin irritation [Warning Skin corrosion/irritation]
Precautionary Statement:	P261, P264, P271, P280, P302+P352, P304+P340, P305+P351+P338, P312, P321, P332+P313, P337+P313, P362, P403+P233, P405, and P501
Signal Word:	Warning

Complexity:	103
Compound Is Canonicalized:	Yes
Covalently-Bonded Unit Count:	1
Defined Atom Stereocenter Count:	0
Defined Bond Stereocenter Count:	0
Exact Mass:	118.053098200
Formal Charge:	0
Heavy Atom Count:	9
Hydrogen Bond Acceptor Count:	1
Hydrogen Bond Donor Count:	1
Isotope Atom Count:	0
Monoisotopic Mass:	118.053098200
Rotatable Bond Count:	0
Topological Polar Surface Area:	28.7 Å²
Undefined Atom Stereocenter Count:	0
Undefined Bond Stereocenter Count:	0
XLogP3:	1