logo
Home  > Chemistry  > Heterocyclic Building Blocks  > Thiophenes  > 5-Bromothiophene-2-carbaldehyde

AB49946

4701-17-1 | 5-Bromothiophene-2-carbaldehyde

Packsize Purity Availability Price Discounted Price    Quantity
1g 98% in stock $6.00 $4.00 -   +
5g 98% in stock $8.00 $5.00 -   +
10g 98% in stock $12.00 $8.00 -   +
25g 98% in stock $22.00 $15.00 -   +
100g 98% in stock $79.00 $55.00 -   +

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

*All prices are in USD.

Description
Catalog Number: AB49946
Chemical Name: 5-Bromothiophene-2-carbaldehyde
CAS Number: 4701-17-1
Molecular Formula: C5H3BrOS
Molecular Weight: 191.0457
MDL Number: MFCD00005432
SMILES: Brc1ccc(s1)C=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: 2.4  

 

 

Upstream Synthesis Route
  • 5-Bromo-2-thiophenecarboxaldehyde is a versatile compound frequently used in chemical synthesis due to its unique properties and reactivity. This compound serves as a valuable building block in the synthesis of various organic compounds, especially in the pharmaceutical and agrochemical industries. One of the key applications of 5-Bromo-2-thiophenecarboxaldehyde is in the preparation of heterocyclic compounds, particularly thiazoles and benzothiazoles. These heterocycles are important structural motifs found in a wide range of biologically active molecules, including pharmaceuticals and natural products. The presence of the bromo group in the molecule allows for further functionalization through cross-coupling reactions, enabling the introduction of additional substituents to tailor the properties of the final compound.Additionally, 5-Bromo-2-thiophenecarboxaldehyde can be utilized in the synthesis of various building blocks for material science applications, such as polymers and optoelectronic materials. Its ability to undergo multiple types of reactions, including nucleophilic addition and condensation reactions, makes it a valuable starting material for the construction of complex molecular architectures.Overall, the versatility and reactivity of 5-Bromo-2-thiophenecarboxaldehyde make it an essential reagent in the toolkit of synthetic chemists for the efficient and targeted construction of diverse organic compounds with potential applications in drug discovery, materials science, and other fields of chemical research.
Literature
FEATURED PRODUCTS