62224-16-2 | Methyl 4-bromothiophene-2-carboxylate

Packsize	Purity	Availability	Price	Discounted Price
1g	95%	in stock	$6.00	$5.00
5g	95%	in stock	$12.00	$9.00
10g	95%	in stock	$22.00	$16.00
25g	95%	in stock	$42.00	$29.00

Description

• Catalog Number: AG73516
• Chemical Name: Methyl 4-bromothiophene-2-carboxylate
• CAS Number: 62224-16-2
• Molecular Formula: C6H5BrO2S
• Molecular Weight: 221.0717
• MDL Number: MFCD06203668
• SMILES: COC(=O)c1cc(cs1)Br

Computed Properties

• Complexity: 140
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 10
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 2
• XLogP3: 2.5

Upstream Synthesis Route

Methyl 4-bromothiophene-2-carboxylate is a versatile compound that finds its application in various chemical synthesis processes. It serves as a valuable building block in the creation of pharmaceuticals, agrochemicals, and materials due to its unique structural properties. In organic synthesis, Methyl 4-bromothiophene-2-carboxylate acts as a precursor for the synthesis of diverse molecules with important biological activities. By undergoing various chemical reactions such as nucleophilic substitution, cross-coupling, or cyclization, this compound can be transformed into more complex structures. Additionally, its bromine and ester functional groups provide opportunities for further derivatization, allowing for the fine-tuning of properties in the final products. Moreover, Methyl 4-bromothiophene-2-carboxylate is utilized in the development of new materials with unique electronic and optoelectronic properties. Its incorporation into polymers or organic semiconductors can enhance their performance in applications such as organic electronic devices or sensors. The presence of the thiophene ring offers favorable π-conjugation, which is beneficial for achieving desired electrical or optical characteristics in the synthesized materials.Overall, the strategic incorporation of Methyl 4-bromothiophene-2-carboxylate in chemical synthesis enables the creation of diverse compounds with potential applications in pharmaceuticals, agrochemicals, and materials science.

Literature

• Synthesis, photochemical synthesis and antitumor evaluation of novel derivatives of thieno[3',2':4,5]thieno[2,3-c]quinolones.

  Chemical & pharmaceutical bulletin 20020501