131474
1-苯基吡咯
99%
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关于此项目
经验公式（希尔记法）:
C10H9N
化学文摘社编号:
分子量:
143.19
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
211-242-3
MDL number:
Assay:
99%
Form:
solid
产品名称
1-苯基吡咯, 99%
InChI key
GEZGAZKEOUKLBR-UHFFFAOYSA-N
InChI
1S/C10H9N/c1-2-6-10(7-3-1)11-8-4-5-9-11/h1-9H
SMILES string
c1ccc(cc1)-n2cccc2
assay
99%
form
solid
bp
234 °C (lit.)
mp
58-60 °C (lit.)
Quality Level
Application
1-Phenylpyrrole was used to study the half-wave potentials of the aqueous redox couples and the oxidation potentials of the monomers in 1,2-dichloroethane.
General description
1-Phenylpyrrole inhibited cytochrome P-450 dependant monooxygenase activity in microsomes from rat liver.
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
T Viswanathan et al.
Journal of medicinal chemistry, 24(7), 822-830 (1981-07-01)
The inhibitions of cytochrome P-450 dependent monooxygenase activity in microsomes from rat liver by 1-phenylpyrrole, 1-(2-isopropylphenyl)pyrrole, 4(5)-phenylimidazole, and 1-(2-isopropylphenyl)imidazole have been compared. The results establish that the presence of an imidazole N-3 nitrogen substituent is not required to inhibit the
Formation of oligomers of methyl-and phenyl-pyrrole at an electrified liquid/liquid interface.
Chemical Communications (Cambridge, England), 19, 2163-2164 (1998)
Kangmin Kim et al.
Journal of the American Chemical Society, 141(15), 6279-6291 (2019-03-28)
Amine-peroxide redox polymerization (APRP) has been highly prevalent in industrial and medical applications since the 1950s, yet the initiation mechanism of this radical polymerization process is poorly understood so that innovations in the field are largely empirically driven and incremental.
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