13932-58-6

Basic information

• Product Name: PYRROLIDINE-1-CARBOXAMIDINE
• Synonyms: pyrrolidine-1-carboximidine;PYRROLIDINE-1-CARBOXAMIDINE(WX684415)
• CAS NO: 13932-58-6
• Molecular Formula: C₅H₁₁N₃
• Molecular Weight: 113.16
• Mol File: 13932-58-6.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 180.3°Cat760mmHg
• Flash Point: 62.8°C
• Appearance: /
• Density: 1.27g/cm³
• Storage Temp.: 2-8°C
• CAS DataBase Reference: PYRROLIDINE-1-CARBOXAMIDINE(CAS DataBase Reference)
• NIST Chemistry Reference: PYRROLIDINE-1-CARBOXAMIDINE(13932-58-6)
• EPA Substance Registry System: PYRROLIDINE-1-CARBOXAMIDINE(13932-58-6)

Safety Data

• Hazardous Substances Data: 13932-58-6(Hazardous Substances Data)

Usage

General Description

PYRROLIDINE-1-CARBOXAMIDINE is a chemical compound with the molecular formula C5H12N2O. It is a derivative of pyrrolidine and is commonly used as a building block in organic synthesis. PYRROLIDINE-1-CARBOXAMIDINE can be used in the pharmaceutical industry for the development of various drugs and medications. It has also been studied for its potential anticonvulsant and antiparasitic properties. Additionally, PYRROLIDINE-1-CARBOXAMIDINE has been investigated for its role in the treatment of neurodegenerative diseases. Overall, this compound has a wide range of potential applications in the field of medicine and chemistry.

InChI:InChI=1/C5H11N3/c6-5(7)8-3-1-2-4-8/h1-4H2,(H3,6,7)/p+1

Upstream product

• 123-75-1 pyrrolidine 
• 49755-46-6 pyrrolidine-1-carboximidamide hydrochloride 
• 38184-47-3 3,5-dimethyl-1-pyrazolylformaminidium nitrate 
• 14527-26-5 2-methylisothiourea sulphate 

Downstream Products

• 120161-06-0 2-(pyrrolidin-1-yl)-1H-benzimidazole 
• 1310552-57-8 methyl-3-(amino(tetrahydro-1H-pyrrolyl)methylenesulfamoyl)-4-bromobenzoate 

Relevant articles and documents

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N1- and N2-Substituted 2-Amino-5,6-dihydro-4(1H)-pyrimidinones (Heterocyclic Compounds, 79)

The reactions of the monosubstituted guanidines 2b-h with methyl acrylate in dimethylformamide or ethanol as solvent preferentially afford 1-substituted 2-amino-5,6-dihydro-4(1H)-pyrimidinones 6b-h.The structures of 1-hexyl- and 1-benzyl-4-pyrimidinones 6c, e and of the picrate of 1-phenylpyrimidinone 6g were proved by comparison with authentic samples, which were prepared from N-substituted ethyl 3-amino-propionates 14c, e and g and cyanamide.Accordingly, 6g is not identical with authentic 2-phenylaminopyrimidinone 7g (prepared from 2-methylthio-4-pyrimidinone 10 and 2-thioxo-4-pyrimidinone 12 respectively, compare.N,N-Disubstituted guanidines 2i-m react with methyl acrylate in dimethylformamide as solvent to afford N2,N2-disubstituted 2-amino-5,6-dihydro-4-(1H)-pyrimidinones 7i-m.Action of morpholine-4-carboxamidine (2l) on methyl acrylate in ethanol yields 2-morpholinopyrimidinone 7l as byproduct and 3-ethoxy-N-propionamide (9l) as mainproduct.Keywords: Acrylic acid methylester, reactions; Guanidines, mono- and N,N-disubstituted; Propionamide, 3-ethoxy-N-; 4(1H)-Pyrimidinones, 2-amino; Pyrimidine-1-propionic acid ethylester, hexahydro-4-oxo-2-thioxo