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CAS 18791-75-8

4-Bromothiophene-2-carboxaldehyde TCI B2827

4-Bromothiophene-2-carboxaldehyde TCI B2827

Chemical Identity

CAS No.
18791-75-8
PubChem
CID 87792·SID 87577972
Formula
C5H3BrOS
Molecular weight
191.05 g/mol
Purity
>98.0%(GC)
Reference databases
ECHA
Full identifiers (IUPAC, SMILES, InChIKey)
IUPAC
4-bromothiophene-2-carbaldehyde
SMILES
C1=C(SC=C1Br)C=O
InChIKey
PDONIKHDXYHTLS-UHFFFAOYSA-N
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4-Bromothiophene-2-carboxaldehyde is a chemical compound widely used as a building block in the synthesis of complex heterocyclic compounds. Its unique structure, containing both sulfur and bromine atoms, makes it a valuable reagent in organic chemistry and pharmaceutical research. This compound is commonly employed in laboratories to construct intricate molecular frameworks, especially in the development of bioactive molecules with therapeutic potential. Due to its structural complexity, it serves as a versatile intermediate in various synthetic pathways.

The compound’s high reactivity, particularly in substitution and condensation reactions, makes it a preferred choice for chemists working on advanced synthetic strategies. The presence of bromine and sulfur atoms contributes to its polarity, enhancing solubility in polar solvents and facilitating efficient chemical reactions. These properties allow it to act as a key substrate in reactions requiring high reactivity and selectivity. Its ability to participate in multiple reaction types also increases its utility in diverse synthetic applications.

In Indonesian laboratories, 4-Bromothiophene-2-carboxaldehyde is commonly used in organic chemistry research, especially in the synthesis of heterocyclic compounds with biological activity. It plays a crucial role in pharmaceutical studies aimed at developing new drugs and bioactive agents. Its application extends to both academic and industrial research settings, supporting the creation of novel chemical structures with potential therapeutic applications.

TCI brochures (PDF)

  • Organic synthesis of heterocyclic compounds due to its reactive functional groups and structural versatility.
  • Pharmaceutical research for the development of bioactive molecules with therapeutic potential.
  • Chemical modification of thiophene derivatives to create new compounds with enhanced pharmacological properties.
  • Investigation of electrophilic substitution reactions in sulfur-containing compounds.
  • Development of novel drug candidates through structural diversification and functional group manipulation.

Brand TCI
CAS number 18791-75-8
Molecular formula —
Purity —
Category Chemistry > Building Blocks > Heterocyclic Building Blocks
Pack sizes Available in standard laboratory quantities
Physical form Solid or liquid depending on the specific product formulation
Storage Store in a cool, dry place away from light and incompatible substances

This compound should be stored in a cool, dry environment, away from direct sunlight and sources of heat. It is recommended to use airtight containers to prevent exposure to moisture and air, which may affect its stability. Due to its reactivity, it should be handled in a well-ventilated area, ideally with appropriate personal protective equipment such as gloves and safety goggles. Avoid contact with incompatible materials, including strong oxidizing agents. Proper labeling and storage in a designated chemical storage cabinet are essential to ensure safety and maintain the integrity of the compound during handling and use.

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