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Assay
97%
form
solid
mp
99-102 °C (lit.)
SMILES string
Cc1ccc(cc1)S(=O)(=O)n2cccc2
InChI
1S/C11H11NO2S/c1-10-4-6-11(7-5-10)15(13,14)12-8-2-3-9-12/h2-9H,1H3
InChI key
OXWIEWFMRVJGNY-UHFFFAOYSA-N
Related Categories
General description
1-(p-Tolylsulfonyl)pyrrole is a pyrrole derivative. Its Fourier-Transform-Infrared, Fourier-Transform-Raman and NMR spectra have been studied.
Application
1-(p-Tolylsulfonyl)pyrrole may be used in the synthesis of 4-(3-pyrrolyl) butanoic aicd (PBA).
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Target Organs
Respiratory system
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Certificates of Analysis (COA)
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Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 146, 88-96 (2015-03-31)
Fourier-Transform-Infrared, Fourier-Transform-Raman and Nuclear Magnetic Rezonans spectra of 1-(p-tolylsulfonyl) pyrrole molecule have been recorded. In the powder form, vibrational spectra of 1-(p-tolylsulfonyl) pyrrol molecule were investigated in the region 4000-400 cm(-1) and 3500-50 cm(-1), respectively. The conformational analysis, geometrical structure
Biosensors & bioelectronics, 20(9), 1821-1828 (2005-02-01)
A simple and label-free electrochemical sensor for recognition of the DNA hybridization event was prepared based on a new functionalised conducting copolymer, poly[pyrrole-co-4-(3-pyrrolyl) butanoic acid]. This precursor copolymer can be easily electrodeposited on the electrode surface and shows high electroactivity
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