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AB50413

1860-99-7 | 2-Bromothiophene-3-carbaldehyde

Packsize Purity Availability Price Discounted Price    Quantity
1g 98% in stock $15.00 $11.00 -   +
5g 98% in stock $61.00 $43.00 -   +
10g 98% in stock $112.00 $79.00 -   +
25g 98% in stock $248.00 $174.00 -   +

*All products are for research use only and not intended for human or animal use.

*All prices are in USD.

Description
Catalog Number: AB50413
Chemical Name: 2-Bromothiophene-3-carbaldehyde
CAS Number: 1860-99-7
Molecular Formula: C5H3BrOS
Molecular Weight: 191.0457
MDL Number: MFCD09025880
SMILES: Brc1sccc1C=O

 

Computed Properties
Complexity: 96.4  
Covalently-Bonded Unit Count: 1  
Heavy Atom Count: 8  
Hydrogen Bond Acceptor Count: 2  
Rotatable Bond Count: 1  
XLogP3: 2.1  

 

 

Upstream Synthesis Route
  • 2-Bromothiophene-3-carbaldehyde, also known as $name$, is a versatile chemical compound widely used in chemical synthesis for various applications. This compound serves as a key building block in the production of pharmaceuticals, agrochemicals, and advanced materials due to its unique reactivity and functional groups.In organic synthesis, $name$ is commonly employed as a precursor in the preparation of heterocyclic compounds and complex molecules. Its distinctive structure containing a bromine atom and an aldehyde group allows for selective functional group transformations, making it a valuable intermediate in the synthesis of diverse organic molecules.Additionally, 2-Bromothiophene-3-carbaldehyde exhibits interesting properties that enable its use in the development of new materials with specific properties. By incorporating this compound into polymerization reactions or surface modifications, scientists can tailor the physical and chemical characteristics of materials for various industrial applications.Moreover, the reactivity of $name$ lends itself to the formation of key intermediates in the synthesis of bioactive compounds and pharmaceuticals. Researchers utilize this compound in the construction of drug candidates and lead compounds, exploiting its unique structural features to introduce specific functional groups and stereochemistry essential for biological activity.Overall, the versatility and reactivity of 2-Bromothiophene-3-carbaldehyde make it a valuable tool in chemical synthesis, enabling the efficient creation of complex molecules, materials, and pharmaceuticals with diverse applications across industries.
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