pyrazolidine
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| Verifiedfields = changed
| Watchedfields = changed
| verifiedrevid = 425120995
| ImageFileL1 = pyrazolidine numbering.png
| ImageClassL1 = skin-invert-image
| ImageSizeL1 = 120px
| ImageAltL1 = Structural formula of pyrazolidine
| ImageFileR1 = Pyrazolidine 3D ball.png
| ImageSizeR1 = 120
| ImageAltR1 = Ball-and-stick model of the pyrazolidine molecule
| PIN = Pyrazolidine{{cite book |author=International Union of Pure and Applied Chemistry |date=2014 |title=Nomenclature of Organic Chemistry: IUPAC Recommendations and Preferred Names 2013 |publisher=The Royal Society of Chemistry |pages=142 |doi=10.1039/9781849733069 |isbn=978-0-85404-182-4}}
| OtherNames = 1,2-Diazolidine
|Section1={{Chembox Identifiers
| CASNo_Ref = {{cascite|correct|??}}
| CASNo =504-70-1
| UNII_Ref = {{fdacite|correct|FDA}}
| UNII = Y0MA3161MR
| PubChem =79033
| SMILES =C1CNNC1
| ChemSpiderID_Ref = {{chemspidercite|changed|chemspider}}
| ChemSpiderID = 71365
| InChI = 1/C3H8N2/c1-2-4-5-3-1/h4-5H,1-3H2
| InChIKey = USPWKWBDZOARPV-UHFFFAOYAM
| StdInChI_Ref = {{stdinchicite|changed|chemspider}}
| StdInChI = 1S/C3H8N2/c1-2-4-5-3-1/h4-5H,1-3H2
| StdInChIKey_Ref = {{stdinchicite|changed|chemspider}}
| StdInChIKey = USPWKWBDZOARPV-UHFFFAOYSA-N
| RTECS =
| MeSHName =
| ChEBI_Ref = {{ebicite|changed|EBI}}
| ChEBI = 33138
}}
|Section2={{Chembox Properties
| Formula =C3H8N2
| MolarMass =72.10902
| Appearance =
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|Section3={{Chembox Hazards
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Pyrazolidine is a heterocyclic compound. It is a liquid that is stable in air, but it is hygroscopic.
Preparation
Pyrazolidine can be produced by cyclization of 1,3-dichloropropane or 1,3-dibromopropane with hydrazine:
:{{chem2 | Cl\s(CH2)3\sCl + N2H4 -> C3H8N2 + 2 HCl }}
:{{chem2 | Br\s(CH2)3\sBr + N2H4 -> C3H8N2 + 2 HBr }}
See also
References
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