cas 2386-33-6|| where to buy 3-Acetyl-4,5-dimethyl-1H-pyrrole-2-carboxylic acid

Product Name:3-Acetyl-4,5-dimethyl-1H-pyrrole-2-carboxylic acid

IUPAC Name:3-acetyl-4,5-dimethyl-1H-pyrrole-2-carboxylic acid

: CAS：2386-33-6; Molecular Formula：C9H11NO3; Purity：95%+

: Catalog Number：CM196901; Molecular Weight：181.19

Packing Unit	Available Stock	Price($)	Quantity
CM196901-25g	in stock	ȀźŔ

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Product Details

: CAS NO:2386-33-6; Molecular Formula:C9H11NO3; Melting Point:-; Smiles Code:CC(=O)C1=C(NC(C)=C1C)C(O)=O; Density:

: Catalog Number:CM196901; Molecular Weight:181.19; Boiling Point:; MDL No:MFCD00734952; Storage:Store at 2-8°C.

Category Infos

: Pyrroles; Pyrrole is a five membered heterocyclic compound with the molecular formula of C4H5N. Pyrrole has a ring composed of four carbon atoms and one nitrogen atom. Pyrrole is easy to polymerize in the air. Pyrrole is the parent compound of many important biological substances (such as bile pigment, porphyrin and chlorophyll). Pyrrole scaffolds are widely used in biological and pharmaceutical fields. Pyrrole is a special heterocyclic scaffold, which exists in many natural products, drug molecules and pesticides, and has shown its application in materials science.; Pyrrole,Where to Buy Pyrroles-Chemenu; Pyrrole,Where to Buy Pyrroles; Pyrrole is a heterocyclic, aromatic, organic compound, a five-membered ring with the formula C 4H 4NH. It is a colorless volatile liquid that darkens readily upon exposure to air. Substituted derivatives are also called pyrroles, e.g., N-methylpyrrole.

Product Other Information

Product Overview	3-Acetyl-4,5-dimethyl-1H-pyrrole-2-carboxylic acid (3-ADPA) is a synthetic organic compound that has been used in a variety of scientific research applications. It is a versatile compound that is used for a wide range of purposes, from catalyzing chemical reactions to being used as a reagent in biochemical and physiological studies. 3-ADPA has been studied extensively, and its unique properties make it an ideal compound for a variety of research purposes.
Synthesis and Application	3-Acetyl-4,5-dimethyl-1H-pyrrole-2-carboxylic acid can be synthesized through a variety of methods. The most common method is the acetylation of 4,5-dimethyl-1H-pyrrole-2-carboxylic acid, which involves the reaction of the acid with acetic anhydride in the presence of a catalyst such as pyridine. Other methods of synthesis include the reaction of 4,5-dimethyl-1H-pyrrole-2-carboxylic acid with acetic acid in the presence of a base, or the reaction of 4,5-dimethyl-1H-pyrrole-2-carboxylic acid with acetyl chloride in the presence of a base. 3-Acetyl-4,5-dimethyl-1H-pyrrole-2-carboxylic acid has been used in a variety of scientific research applications. It has been used as a reagent for the synthesis of a variety of compounds, including heterocyclic compounds and pharmaceuticals. It has also been used as a catalyst for a variety of chemical reactions, including the synthesis of amino acids and peptides. Additionally, 3-Acetyl-4,5-dimethyl-1H-pyrrole-2-carboxylic acid has been used as a reagent in biochemical and physiological studies, such as the study of protein-protein interactions and the study of enzyme activity.
Future Directions	The potential applications of 3-Acetyl-4,5-dimethyl-1H-pyrrole-2-carboxylic acid are vast and varied. It has been studied extensively for its use in biochemical and physiological studies, and its potential for use in drug development is being explored. Additionally, the use of 3-Acetyl-4,5-dimethyl-1H-pyrrole-2-carboxylic acid in the synthesis of heterocyclic compounds and pharmaceuticals is being investigated. Finally, the use of 3-Acetyl-4,5-dimethyl-1H-pyrrole-2-carboxylic acid in the synthesis of amino acids and peptides is being explored.