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Details

Stereochemistry ACHIRAL
Molecular Formula C3H8N2
Molecular Weight 72.109
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of PYRAZOLIDINE

SMILES

C1CNNC1

InChI

InChIKey=USPWKWBDZOARPV-UHFFFAOYSA-N
InChI=1S/C3H8N2/c1-2-4-5-3-1/h4-5H,1-3H2

HIDE SMILES / InChI

Molecular Formula C3H8N2
Molecular Weight 72.109
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Synthesis and properties of chiral pyrazolidines derived from (+)-pulegone.
2010-07-05
Skeletally diverse small molecules using a build/couple/pair strategy.
2009-04-02
Efficient air-stable organometallic low-molecular-mass gelators for ionic liquids: synthesis, aggregation and application of pyridine-bridged bis(benzimidazolylidene)-palladium complexes.
2009
Stereoselective synthesis of cis- or trans-3,5-disubstituted pyrazolidines via Pd-catalyzed carboamination reactions: use of allylic strain to control product stereochemistry through N-substituent manipulation.
2008-10-01
5-(3-Fluoro-phen-yl)-1-phenyl-pyrazolidin-3-one.
2008-09-06
Regioselective synthesis of 1,3,5-tri- and 1,3,4,5-tetrasubstituted pyrazoles from N-arylhydrazones and nitroolefins.
2008-03-21
2'-(4-Chlorophenyl)-2,3,4,5,6,7-hexahydro-4',7'-methanospiro[9H-fluorene-9,3'-1H-indazole]-1'-carbonitrile and methyl 4'-chloro-2'-(4-chlorophenyl)-1'-cyanospiro[9H-fluorene-9,3'-pyrazolidine]-4'-carboxylate.
2007-12
GaCl(3)-catalyzed insertion of diazene derivatives into the cyclopropane ring.
2007-09-28
Highly diastereoselective palladium-catalyzed cyclizations of 3,4-allenylic hydrazines and organic halides -- highly stereoselective synthesis of optically active pyrazolidine derivatives and the prediction of the stereoselectivity.
2007
Aqueous N-heterocyclization of primary amines and hydrazines with dihalides: microwave-assisted syntheses of N-azacycloalkanes, isoindole, pyrazole, pyrazolidine, and phthalazine derivatives.
2006-01-06
Stereoselective palladium-catalyzed four-component cascade synthesis of pyrrolidinyl-, pyrazolidinyl-, and isoxazolidinyl isoquinolines.
2005-11-25
Specialist gelator for ionic liquids.
2005-11-08
Pyrazolidine derivatives with heteroaryl urea as dipeptidyl peptidase IV inhibitors.
2005-08
Inhibition of dipeptidyl peptidase IV by novel inhibitors with pyrazolidine scaffold.
2005-07-01
Synthesis and antibacterial activity of dihydro-1,2-oxazine and 2-pyrazoline oxazolidinones: novel analogs of linezolid.
2005-06-02
Synthesis and evaluation of pyrazolidine derivatives as dipeptidyl peptidase IV (DP-IV) inhibitors.
2005-03-01
Metabolism, pharmacokinetics, tissue distribution, and excretion of [14C]CP-424391 in rats.
2005-01
Zirconium-catalyzed enantioselective [3+2] cycloaddition of hydrazones to olefins leading to optically active pyrazolidine, pyrazoline, and 1,3-diamine derivatives.
2004-09-15
Cu- and Pd-catalyzed asymmetric one-pot tandem addition-cyclization reaction of 2-(2',3'-alkadienyl)-beta-keto esters, organic halides, and dibenzyl azodicarboxylate: an effective protocol for the enantioselective synthesis of pyrazolidine derivatives.
2004-06-24
Asymmetric intramolecular [3 + 2] cycloaddition reactions of acylhydrazones/olefins using a chiral zirconium catalyst.
2002-11-20
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 19:56:00 GMT 2025
Edited
by admin
on Mon Mar 31 19:56:00 GMT 2025
Record UNII
Y0MA3161MR
Record Status Validated (UNII)
Record Version
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Name Type Language
PYRAZOLIDINE
Preferred Name English
Code System Code Type Description
PUBCHEM
79033
Created by admin on Mon Mar 31 19:56:00 GMT 2025 , Edited by admin on Mon Mar 31 19:56:00 GMT 2025
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CAS
504-70-1
Created by admin on Mon Mar 31 19:56:00 GMT 2025 , Edited by admin on Mon Mar 31 19:56:00 GMT 2025
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CHEBI
33138
Created by admin on Mon Mar 31 19:56:00 GMT 2025 , Edited by admin on Mon Mar 31 19:56:00 GMT 2025
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EPA CompTox
DTXSID30198444
Created by admin on Mon Mar 31 19:56:00 GMT 2025 , Edited by admin on Mon Mar 31 19:56:00 GMT 2025
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FDA UNII
Y0MA3161MR
Created by admin on Mon Mar 31 19:56:00 GMT 2025 , Edited by admin on Mon Mar 31 19:56:00 GMT 2025
PRIMARY
WIKIPEDIA
PYRAZOLIDINE
Created by admin on Mon Mar 31 19:56:00 GMT 2025 , Edited by admin on Mon Mar 31 19:56:00 GMT 2025
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