83242
Pyrrolidine
purum, ≥98.0% (GC)
Synonym(s):
Tetrahydropyrrole, Tetramethyleneimine
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About This Item
Empirical Formula (Hill Notation):
C4H9N
CAS Number:
Molecular Weight:
71.12
EC Number:
204-648-7
UNSPSC Code:
12352100
MDL number:
Beilstein/REAXYS Number:
102395
vapor density
2.45 (vs air)
vapor pressure
128 mmHg ( 39 °C), 49 mmHg ( 20 °C)
grade
purum
assay
≥98.0% (GC)
autoignition temp.
653 °F
expl. lim.
10.6 %
impurities
≤1% water
refractive index
n20/D 1.443 (lit.), n20/D 1.444
density
0.852 g/mL at 25 °C (lit.)
SMILES string
C1CCNC1
InChI
1S/C4H9N/c1-2-4-5-3-1/h5H,1-4H2
InChI key
RWRDLPDLKQPQOW-UHFFFAOYSA-N
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Xueqing Zhao et al.
Bioorganic & medicinal chemistry, 21(2), 470-484 (2012-12-19)
A series of enantiomerically pure 4-hydroxy-4-(4-methoxyphenyl)-substituted proline and pyrrolidin-2-ylacetic acid derivatives have been synthesized starting from the respective N-protected 4-hydroxy derivatives via oxidation to the corresponding 4-oxo compounds, subsequent addition of organometallic reagents, final hydrolysis and deprotection. The major diastereoisomers
Boyu Zhang et al.
Angewandte Chemie (International ed. in English), 51(52), 13159-13162 (2012-11-20)
Drop it! A highly enantioselective catalytic cascade reaction of α-ketoacids and aldehydes is achieved using the title catalyst and water as the solvent. Fluorescence imaging shows that the catalyst is mainly distributed on the surface of emulsion droplets. Optically active
Dongbo Mi et al.
Journal of nanoscience and nanotechnology, 13(5), 3474-3479 (2013-07-19)
Currently, [60] fullerene derivatives are the focus of considerable research due to their important roles in many fields, especially material science. In this study, we synthesized the following two novel fulleropyrrolidine derivatives: C60-fused N-methyl-(4-hexyloxybenzen-2-yl) pyrrolidine, (p-HOPF) and C60-fused N-methyl-(2-hexyloxybenzen-2-yl) pyrrolidine
Aiko Nitta et al.
Bioorganic & medicinal chemistry letters, 22(22), 6876-6881 (2012-10-11)
Optimization starting with our lead compound 1 (IC(50)=4.9 nM) led to the identification of pyrrolidinyl phenylurea derivatives. Further modification toward improvement of the bioavailability provided (R)-1-(1-((6-fluoronaphthalen-2-yl)methyl)pyrrolidin-3-yl)-3-(2-(2-hydroxyethoxy)phenyl)urea 32 (IC(50)=1.7 nM), a potent and orally active CCR3 antagonist.
Gürkan Keşan et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 101, 22-30 (2012-10-27)
FT-IR and Raman spectra of 1-pyrrolidino-1-cyclopentene (1py1cp) were experimentally reported in the region of 4000-10 cm(-1) and 4000-100 cm(-1), respectively. The optimized geometric parameters, normal mode frequencies and corresponding vibrational assignments of 1py1cp (C9H15N) were theoretically examined by means of
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