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131474

Sigma-Aldrich

1-Phenylpyrrole

99%

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About This Item

Empirical Formula (Hill Notation):
C10H9N
CAS Number:
635-90-5
Molecular Weight:
143.19
EC Number:
211-242-3
MDL number:
MFCD00005343
UNSPSC Code:
12352100
PubChem Substance ID:
24848017
NACRES:
NA.22

Quality Level

100

Assay

99%

form

solid

bp

234 °C (lit.)

mp

58-60 °C (lit.)

SMILES string

c1ccc(cc1)-n2cccc2

InChI

1S/C10H9N/c1-2-6-10(7-3-1)11-8-4-5-9-11/h1-9H

InChI key

GEZGAZKEOUKLBR-UHFFFAOYSA-N

Related Categories

General description

1-Phenylpyrrole inhibited cytochrome P-450 dependant monooxygenase activity in microsomes from rat liver.

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.

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H315,H319,H335

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

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

JAN Code

131474-25G:
131474-VAR:
131474-10G:
131474-1KG:
131474-BULK:

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Certificates of Analysis (COA)

Lot/Batch Number
STBK1762
STBJ8769
STBJ2956
STBH8129
STBH1545

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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.

Global Trade Item Number

SKUGTIN
131474-10G4061833464502
131474-25G

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