7311-63-9 | 5-Bromothiophene-2-carboxylic acid

Packsize	Purity	Availability	Price	Discounted Price
5g	97%	in stock	$13.00	$9.00
10g	97%	in stock	$15.00	$10.00
25g	97%	in stock	$25.00	$17.00

Description

• Catalog Number: AB69043
• Chemical Name: 5-Bromothiophene-2-carboxylic acid
• CAS Number: 7311-63-9
• Molecular Formula: C5H3BrO2S
• Molecular Weight: 207.0451
• MDL Number: MFCD00079725
• SMILES: OC(=O)c1ccc(s1)Br
• NSC Number: 408675

Computed Properties

• Complexity: 128
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 9
• Hydrogen Bond Acceptor Count: 3
• Hydrogen Bond Donor Count: 1
• Rotatable Bond Count: 1
• XLogP3: 2.5

Upstream Synthesis Route

5-Bromothiophene-2-carboxylic acid is a versatile compound that plays a crucial role in chemical synthesis. It is commonly employed as a building block in the preparation of various organic molecules due to its unique reactivity and structural properties. In the realm of organic chemistry, this compound serves as a valuable intermediate in the synthesis of diverse pharmaceuticals, agrochemicals, and materials.As a key reagent in the field of medicinal chemistry, 5-Bromothiophene-2-carboxylic acid facilitates the creation of novel drug candidates through the formation of important chemical bonds and functional groups. Its incorporation into drug molecules can enhance their biological activity, improve pharmacokinetic properties, and allow for targeted drug delivery. Furthermore, this compound is utilized in the synthesis of specialty chemicals, such as dyes, polymers, and electronic materials, where its specific structure imparts desired chemical and physical properties to the final products.By serving as a key building block in chemical synthesis, 5-Bromothiophene-2-carboxylic acid enables the creation of diverse molecular architectures with tailored functionalities and applications. Its versatility and reactivity make it a valuable tool for researchers and chemists working in various fields, driving innovation and enabling the development of new and exciting materials and compounds.

Literature

• Ionic immobilization, diversification, and release: application to the generation of a library of methionine aminopeptidase inhibitors.

  Journal of combinatorial chemistry 20080101

• Prediction of genotoxicity of chemical compounds by statistical learning methods.

  Chemical research in toxicology 20050601