5-Formyl-2,4-dimethyl-1H-pyrrole-3-carboxylic Acid CAS NO.:253870-02-9

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5-Formyl-2,4-dimethyl-1H-pyrrole-3-carboxylic Acid CAS NO.:253870-02-9
Details
5-Formyl-2,4-dimethyl-1H-pyrrole-3-carboxylic acid 5-Formyl-2,4-dimethyl-1H-pyrrole-3-carboxylic acid Usage
Category
Other Intermediates
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Description
5-Formyl-2,4-dimethyl-1H-pyrrole-3-carboxylic acid
Product Name:
5-Formyl-2,4-dimethyl-1H-pyrrole-3-carboxylic acid
Synonyms:
5-FORMYL-2,4-DIMETHYL-1H-PYRROLE-3-CARBOXYLICACID;3,5-DIMETHYL-2-FORMYLPYRROLE-4-CARBOXYLICACID;5-Formyl-2,4-dimethylpyrrole-3-carboxylicacid;5-FORMYL-2,4-DIMETHYL-1H-PYRRChemicalbookOLE-3-CARBOXYLICACID98%;5-formyl-2,4-dimethyl-1h-pyrrole-3-carboxyacid;
5-ForMyl-2,4-diMethyl-1H-;2,4-Dimethyl-5-formyl-1H-pyrrole-3-carboxylicacid97%;SunitinibinterMediate
CAS:
253870-02-9
MF:
C8H9NO3
MW:
167.16
EINECS
607-716-8
5-Formyl-2,4-dimethyl-1H-pyrrole-3-carboxylic acid
Melting point
283°C(lit.)
Density
1.342±0.06 g/cm3(Predicted)
Boiling point
374.9±42.0 °C(Predicted)
Apk
5.56±0.50(Predicted)
Solubility
Alkaline solution (slightly soluble), DMSO (slightly soluble), methanol (slightly soluble)
Storage temp.
Keep in dark place,Sealed in dry,Room Temperature
Form
solid 
Color
 beige
5-Formyl-2,4-dimethyl-1H-pyrrole-3-carboxylic acid Usage
Uses
1. Used in synthesizing pharmaceutical intermediates: This compound contains a pyrrole ring, which is a core structural unit in many bioactive natural products and drug molecules. Its aldehyde, carboxyl and methyl groups can participate in building pharmaceutically active intermediates through derivatization reactions, potentially for synthesizing antibacterial, anti-inflammatory or anti-tumor candidate drugs.
2. As an organic synthesis intermediate: The multiple functional groups of 2,4-dimethyl-5-formyl-1H-pyrrole-3-carboxylic acid have strong reactivity. They can participate in synthesizing various complex organic compounds through condensation, esterification, substitution and other reactions, serving as an important precursor for synthesizing multiple pyrrole derivatives.
3. Used in the field of material chemistry: Due to its conjugated structure of the pyrrole ring and multiple reactive functional groups, it is presumed to be applicable in synthesizing conjugated polymer materials or functional dyes, with the prospect of preparing materials with photoelectric properties and playing a role in material chemistry.

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