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Merck

131474

Sigma-Aldrich

1-苯基吡咯

99%

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About This Item

经验公式(希尔记法):
C10H9N
CAS号:
分子量:
143.19
EC號碼:
MDL號碼:
分類程式碼代碼:
12352100
PubChem物質ID:
NACRES:
NA.22

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.

象形圖

Exclamation mark

訊號詞

Warning

危險聲明

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


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Slide 1 of 2

1 of 2

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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