1-(2-Pyridyl)piperazine - CAS 34803-66-2

Catalog:	BB022293
Product Name:	1-(2-Pyridyl)piperazine
CAS:	34803-66-2
Synonyms:	1-Pyridin-2-yl-piperazine; N-(2-pyridyl)piperazine

Technical Data

Safety and Hazards

Patents

Literatures

Computed Properties

IUPAC Name:	1-pyridin-2-ylpiperazine
Description:	1-(2-Pyridyl)piperazine is a selective α2-adrenoceptor antagonist. It shows sympatholytic activity.
Molecular Weight:	163.22
Molecular Formula:	C9H13N3
Canonical SMILES:	C1CN(CCN1)C2=CC=CC=N2
InChI:	InChI=1S/C9H13N3/c1-2-4-11-9(3-1)12-7-5-10-6-8-12/h1-4,10H,5-8H2
InChI Key:	GZRKXKUVVPSREJ-UHFFFAOYSA-N
Boiling Point:	293 °C
Purity:	> 98 %
Density:	1.072 g/cm³
Appearance:	Clear colourless to yellow liquid
MDL:	MFCD00006216
LogP:	0.88500

Publication Number	Title	Priority Date
WO-2021079962-A1	Pharmaceutical composition for prevention and/or treatment of hearing loss	20191024
WO-2021055744-A1	4-substituted indole and indazole sulfonamido derivatives as parg inhibitors	20190920
WO-2021034087-A1	Novel compound having cancer metastasis inhibitory activity, preparation method therefor, and pharmaceutical composition for inhibiting cancer metastasis and invasion or treating colorectal cancer, comprising compound	20190819
US-2020407609-A1	Moisture curable polyurethane hot melt adhesive composition having low levels of diisocyanate monomer	20190625
WO-2020264159-A1	Moisture curable polyurethane hot melt adhesive composition having low levels of diisocyanate monomer	20190625

PMID	Publication Date	Title	Journal
22931884	20120801	[Determination of methyl isocyanate (MIC) in air of workplaces by HPLC]	Zhonghua lao dong wei sheng zhi ye bing za zhi = Zhonghua laodong weisheng zhiyebing zazhi = Chinese journal of industrial hygiene and occupational diseases
22624326	20120301	Synthesis of s-triazine-based thiazolidinones as antimicrobial agents	Zeitschrift fur Naturforschung. C, Journal of biosciences
21507636	20110515	A novel series of piperazinyl-pyridine ureas as antagonists of the purinergic P2Y12 receptor	Bioorganic & medicinal chemistry letters
21773062	20110401	Synthesis and Biological Evaluation of New 3-Phenyl-1-[(4-arylpiperazin-1-yl)alkyl]-piperidine-2,6-diones	Scientia pharmaceutica
21290451	20110315	Piperazines for peptide carboxyl group derivatization: effect of derivatization reagents and properties of peptides on signal enhancement in matrix-assisted laser desorption/ionization mass spectrometry	Rapid communications in mass spectrometry : RCM

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Related Functional Groups

Piperazines

[1217482-26-2]
(R)-piperazin-2-ylmethanol dihydrochloride
[1197236-47-7]
Ethyl 4-[2-(4-amino-3-methylpyrazol-1-yl)propanoyl]piperazine-1-carboxylate hydrochloride
[1423024-26-3]
N''-(piperazine-1-carboximidoyl)guanidine trihydrochloride
[402832-69-3]
(2S,6S)-2,6-Dimethylpiperazine
[7755-92-2]
1-Formylpiperazine
[761440-26-0]
1-(3-Methoxy-4-nitrophenyl)-4-methylpiperazine

Pyridines

[149463-07-0]
2-(Chloromethyl)-3-fluoropyridine Hydrochloride
[153259-31-5]
2-(Chloromethyl)-4-(3-methoxypropoxy)-3-methylpyridine Hydrochloride
[1261365-99-4]
2,5-Dichloro-6-(hydroxymethyl)pyridin-3-ol
[267242-99-9]
2-Chloro-4-methyl-6,7-dihydro-5H-cyclopenta[b]pyridine
[63585-69-3]
2-Methyl-3-nitropyridine Hydrochloride
[1198098-45-1]
3-Allyl-5-methyl-1H-pyrrolo[2,3-b]pyridine

GHS Hazard Statement:	H314 (12.24%): Causes severe skin burns and eye damage [Danger Skin corrosion/irritation]
Precautionary Statement:	P260, P261, P264, P271, P280, P301+P330+P331, P302+P352, P303+P361+P353, P304+P340, P305+P351+P338, P310, P312, P321, P332+P313, P337+P313, P362, P363, P403+P233, P405, and P501
Signal Word:	Danger

Complexity:	132
Compound Is Canonicalized:	Yes
Covalently-Bonded Unit Count:	1
Defined Atom Stereocenter Count:	0
Defined Bond Stereocenter Count:	0
Exact Mass:	163.110947427
Formal Charge:	0
Heavy Atom Count:	12
Hydrogen Bond Acceptor Count:	3
Hydrogen Bond Donor Count:	1
Isotope Atom Count:	0
Monoisotopic Mass:	163.110947427
Rotatable Bond Count:	1
Topological Polar Surface Area:	28.2 Å²
Undefined Atom Stereocenter Count:	0
Undefined Bond Stereocenter Count:	0
XLogP3:	0.7