Pyrrole-3-carboxylic acid, 98+%
Pyrrole-3-carboxylic acid, 98+%
Pyrrole-3-carboxylic acid, 98+%
Thermo Scientific Chemicals

Pyrrole-3-carboxylic acid, 98+%

CAS: 931-03-3 | C5H5NO2 | 111.1 g/mol
数量:
250 mg
1 g
5 g
製品番号(カタログ番号) H55383.MD
または、製品番号H55383-MD
価格(JPY)
-
数量:
250 mg
一括またはカスタム形式をリクエストする
化学物質識別子
CAS931-03-3
IUPAC Name1H-pyrrole-3-carboxylic acid
Molecular FormulaC5H5NO2
InChI KeyDOYOPBSXEIZLRE-UHFFFAOYSA-N
SMILESOC(=O)C1=CNC=C1
さらに表示
FormOff-white to yellow
FormPowder or crystals or crystalline powder
Assay from Suppliers CofA≥98.0%
Pyrrole-3-carboxylic acid is useful for the synthesis of cholecystokinin antagonists, benzopyran antihypertensives and azepinediones. It is utilized for the preparation of a poly(pyrrole-3-carboxylic acid) modified pencil graphite electrode and its usage in the determination of serotonin (SER) in blood serum and urine samples.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
Pyrrole-3-carboxylic acid is useful for the synthesis of cholecystokinin antagonists, benzopyran antihypertensives and azepinediones. It is utilized for the preparation of a poly(pyrrole-3-carboxylic acid) modified pencil graphite electrode and its usage in the determination of serotonin (SER) in blood serum and urine samples.

Solubility
Soluble in water.

Notes
Incompatible with strong bases, strong oxidizing agents, strong reducing agents.
RUO – Research Use Only

General References:

  1. Lee, J. S.; Kim, M.; Oh, J.; Kim, J.; Cho, S.; Jun, J.; Jang, J. Platinum-decorated carbon nanoparticle/polyaniline hybrid paste for flexible wideband dipole tag-antenna application. J. Mater. Chem. A 2015, 3 (13), 7029-7035.
  2. Estévez, V.; Villacampa, M.; Menéndez, C. J. Recent advances in the synthesis of pyrroles by multicomponent reactions. Chem. Soc. Rev. 2014, 43 (13), 4633-4657.