Produktname:4-Bromobenzo[b]thiophene

IUPAC Name:4-bromo-1-benzothiophene

CAS:5118-13-8
Molekulare Formel:C8H5BrS
Reinheit:95%+
Katalognummer:CM103683
Molekulargewicht:213.09

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Produkt-Details

CAS-Nr.:5118-13-8
Molekulare Formel:C8H5BrS
Schmelzpunkt:-
SMILES-Code:BrC1=C(C=CS2)C2=CC=C1
Dichte:
Katalognummer:CM103683
Molekulargewicht:213.09
Siedepunkt:284.7°C at 760 mmHg
Mdl-Nr.:MFCD08669544
Lagerung:RT, protect from light

Category Infos

Benzothiophenes
Benzothiophene is an aromatic organic compound with the molecular formula C8H6S and a naphthalene-like odor. Benzothiophenes are used in research as a starting material for the synthesis of larger, often biologically active structures. It exists in medicinal chemical structures such as raloxifene, zileuton, and sertaconazole, and can also be found in BTCP. It is also used to make dyes such as thioindigo.

Column Infos

Benzo Heterocycles
Benzoheterocycles are heterocycles which are fused with a benzene ring. Coumarone, thianaphthene, benzopyridine, isoquinoline, and dibenzopyridine all belong to this class of compounds.

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Product Other Information

Product Overview 4-Bromobenzo[b]thiophene (4-BBT) is a sulfur-containing heterocyclic compound and a member of the thiophene family. 4-BBT has been studied extensively for its potential applications in organic synthesis, drug design, and materials science. In particular, 4-BBT has been used as a starting material in the synthesis of various pharmaceuticals, including antibiotics and anti-cancer agents. In addition, 4-BBT has been studied for its potential use in the development of new materials with improved properties, such as high-temperature stability and enhanced electrical conductivity.
Synthesis and Application 4-Bromobenzo[b]thiophene can be synthesized by a variety of methods, including the Williamson ether synthesis, the Knoevenagel condensation, and the Friedel-Crafts alkylation. The most common method for the synthesis of 4-Bromobenzo[b]thiophene is the Williamson ether synthesis, which involves the reaction of 4-bromobenzaldehyde and thiophene-2-thiol in the presence of a base, such as sodium hydroxide or potassium carbonate. This reaction yields 4-Bromobenzo[b]thiophene in high yield and purity. 4-Bromobenzo[b]thiophene has been studied extensively for its potential applications in organic synthesis, drug design, and materials science. It has been used as a starting material in the synthesis of various pharmaceuticals, including antibiotics and anti-cancer agents. In addition, 4-Bromobenzo[b]thiophene has been studied for its potential use in the development of new materials with improved properties, such as high-temperature stability and enhanced electrical conductivity.
Future Directions The potential applications of 4-Bromobenzo[b]thiophene are vast, and further research is needed to explore its full potential. Future research should focus on the development of new synthetic methods for the synthesis of 4-Bromobenzo[b]thiophene, as well as the elucidation of its mechanism of action. In addition, further research should explore the potential therapeutic applications of 4-Bromobenzo[b]thiophene, such as its potential use as an antioxidant and antimicrobial agent. Finally, further research should aim to optimize the properties of 4-Bromobenzo[b]thiophene-based materials, such as its thermal and electrical properties, for use in a variety of applications.