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品質等級
化驗
99%
形狀
solid
bp
234 °C (lit.)
mp
58-60 °C (lit.)
SMILES 字串
c1ccc(cc1)-n2cccc2
InChI
1S/C10H9N/c1-2-6-10(7-3-1)11-8-4-5-9-11/h1-9H
InChI 密鑰
GEZGAZKEOUKLBR-UHFFFAOYSA-N
一般說明
1-Phenylpyrrole inhibited cytochrome P-450 dependant monooxygenase activity in microsomes from rat liver.
應用
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.
訊號詞
Warning
危險分類
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
標靶器官
Respiratory system
儲存類別代碼
11 - Combustible Solids
水污染物質分類(WGK)
WGK 3
閃點(°F)
Not applicable
閃點(°C)
Not applicable
個人防護裝備
dust mask type N95 (US), Eyeshields, Gloves
其他客户在看
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)
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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