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3-Pyrroline

CAS No.:
109-96-6
Catalog Number:
AG0033S8
Molecular Formula:
C4H7N
Molecular Weight:
69.1051
Pack Size
Purity
Availability
Location
Price(USD)
Quantity
  
1g
70%
In Stock USA
United States
$78
- +
5g
70%
In Stock USA
United States
$207
- +
Product Description
Catalog Number:
AG0033S8
Chemical Name:
3-Pyrroline
CAS Number:
109-96-6
Molecular Formula:
C4H7N
Molecular Weight:
69.1051
MDL Number:
MFCD00005213
IUPAC Name:
2,5-dihydro-1H-pyrrole
InChI:
InChI=1S/C4H7N/c1-2-4-5-3-1/h1-2,5H,3-4H2
InChI Key:
JVQIKJMSUIMUDI-UHFFFAOYSA-N
SMILES:
N1CC=CC1
EC Number:
203-723-1
UNII:
N0KYF81SDY
NSC Number:
89295
Properties
Complexity:
41.6  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
69.058g/mol
Formal Charge:
0
Heavy Atom Count:
5  
Hydrogen Bond Acceptor Count:
1  
Hydrogen Bond Donor Count:
1  
Isotope Atom Count:
0
Molecular Weight:
69.107g/mol
Monoisotopic Mass:
69.058g/mol
Rotatable Bond Count:
0
Topological Polar Surface Area:
12A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
0
Literature
Title Journal
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Biodegradation of the major color containing compounds in distillery wastewater by an aerobic bacterial culture and characterization of their metabolites. Biodegradation 20100901
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Total synthesis of uniflorine A, casuarine, australine, 3-epi-australine, and 3,7-di-epi-australine from a common precursor. The Journal of organic chemistry 20100205
Formation of N-alkylpyrroles via intermolecular redox amination. Journal of the American Chemical Society 20091125
An efficient synthetic approach to polycyclic 2,5-dihydropyrroles from alpha-silyloxy ketones. The Journal of organic chemistry 20091106
Zn and Fe complexes containing a redox active macrocyclic biquinazoline ligand. Inorganic chemistry 20090406
Annulations of enantioenriched allenylsilanes with in situ generated iminium ions: stereoselective synthesis of diverse heterocycles. Organic letters 20090115
Knorr-Rabe partial reduction of pyrroles: application to the synthesis of indolizidine alkaloids. Beilstein journal of organic chemistry 20080101
Identification of novel chemical inhibitors for ubiquitin C-terminal hydrolase-L3 by virtual screening. Bioorganic & medicinal chemistry 20071101
Microwave-assisted preparations of dihydropyrroles from alkenone O-phenyl oximes. Chemical communications (Cambridge, England) 20071021
TD-DFT investigation of diarylethene dyes with cyclopentene, dihydrothiophene, and dihydropyrrole bridges. The journal of physical chemistry. A 20070628
The double reduction of cyclic sulfonamides for the synthesis of (4S-Phenylpyrrolidin-2R-yl)methanol and 2S-methyl-4S-phenylpyrrolidine. The Journal of organic chemistry 20070302
Highly potent 3-pyrroline mechanism-based inhibitors of bovine plasma amine oxidase and mass spectrometric confirmation of cofactor derivatization. Bioorganic & medicinal chemistry 20070215
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Design and synthesis of a 3,4-dehydroproline amide discovery library. Journal of combinatorial chemistry 20070101
Efficient approach to the Azaspirane core of FR 901483. Organic letters 20061012
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Molecular structure of 2,5-dihydropyrrole (C4NH7), obtained by gas-phase electron diffraction and theoretical calculations. The journal of physical chemistry. A 20050609
In vitro antifungal activity of 2-(3,4-dimethyl-2,5-dihydro-1H-pyrrol-2-yl)-1-methylethyl pentanoate, a dihydropyrrole derivative. Journal of medical microbiology 20050601
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Synthesis of 4-aryl-2-pyrrolidones and beta-aryl-gamma-amino-butyric acid (GABA) analogues by Heck arylation of 3-pyrrolines with arenediazonium tetrafluoroborates. Synthesis of (+/-)-rolipram on a multigram scale and chromatographic resolution by semipreparative chiral simulated moving bed chromatography. The Journal of organic chemistry 20050204
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Solvent-dependent chemoselectivities in additions of beta-carbonyl imines to allyltrimethylsilane with CTAN. The Journal of organic chemistry 20040917
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Fragmentation patterns of novel dispirocyclopiperazinium dibromides with strong analgesic activity under electrospray ionization tandem mass spectrometry conditions. Rapid communications in mass spectrometry : RCM 20040101
Synthesis and insecticidal activity of novel N-oxydihydropyrrole derivatives with a substituted spirocyclohexyl group. Bioscience, biotechnology, and biochemistry 20030601
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Synthesis and insecticidal activity of novel dihydropyrrole derivatives with N-sulfanyl, sulfinyl, and sulfonyl moieties. Bioorganic & medicinal chemistry 20030220
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3-pyrrolines are mechanism-based inactivators of the quinone-dependent amine oxidases but only substrates of the flavin-dependent amine oxidases. Journal of the American Chemical Society 20021016
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Enantioselective total syntheses of manzamine a and related alkaloids. Journal of the American Chemical Society 20020724
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A convenient method for 3-pyrroline synthesis. Organic letters 20011018
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Properties