Product Name:3-bromo-6H-thieno[2,3-b]pyrrole-5-carboxylic acid

IUPAC Name:3-bromo-6H-thieno[2,3-b]pyrrole-5-carboxylic acid

CAS:1007386-45-9
Molecular Formula:C7H4BrNO2S
Purity:95%+
Catalog Number:CM362613
Molecular Weight:246.08

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CM362613-1g 6-8 Weeks ŹŗȎNJ

For R&D use only.

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Product Details

CAS NO:1007386-45-9
Molecular Formula:C7H4BrNO2S
Melting Point:-
Smiles Code:OC(=O)C1=CC2=C(N1)SC=C2Br
Density:
Catalog Number:CM362613
Molecular Weight:246.08
Boiling Point:
MDL No:
Storage:

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.
Thiophenes
Thiophene is a five-membered heterocyclic compound containing a sulfur heteroatom with the molecular formula C4H4S. Thiophene is aromatic and is very similar to benzene; electrophilic substitution reaction is easier than benzene, and it is mainly substituted at the 2-position. Thiophene ring system has certain stability to oxidant.

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Product Other Information

Product Overview 3-bromo-6H-thieno[2,3-b]pyrrole-5-carboxylic acid is a heterocyclic organic compound that has been widely studied for its potential applications in the field of medicinal chemistry. This compound is a member of the thienopyrrole family, which is known for its diverse biological activities.
Synthesis and Application One of the most common synthesis methods of 3-bromo-6H-thieno[2,3-b]pyrrole-5-carboxylic acid involves the reaction of 3-bromo-2-thiophenecarboxaldehyde with 2-cyanopyrrole in the presence of a base such as potassium carbonate. This reaction leads to the formation of the desired product in good yields. Other methods involve the use of different starting materials and reaction conditions. 3-bromo-6H-thieno[2,3-b]pyrrole-5-carboxylic acid has been studied for its potential applications in the field of medicinal chemistry. It has been shown to possess a wide range of biological activities, including antitumor, anti-inflammatory, and antimicrobial properties.
Future Directions There are several future directions for the research on 3-bromo-6H-thieno[2,3-b]pyrrole-5-carboxylic acid. One direction is to continue to explore its potential applications in the field of medicinal chemistry, particularly in the development of new drugs for the treatment of cancer and inflammatory diseases. Another direction is to study its mechanism of action in more detail, with the aim of identifying new targets for drug discovery. Finally, more studies are needed to investigate its potential side effects and toxicity, in order to ensure its safety for clinical use.