4815-35-4 | 2-Amino-5-phenyl-thiophene-3-carboxylic acid amide

Packsize	Purity	Availability	Price	Discounted Price
1g	96%	in stock	$100.00	$70.00
5g	96%	in stock	$297.00	$208.00
10g	96%	in stock	$448.00	$314.00
25g	96%	in stock	$758.00	$531.00

Description

• Catalog Number: AG26319
• Chemical Name: 2-Amino-5-phenyl-thiophene-3-carboxylic acid amide
• CAS Number: 4815-35-4
• Molecular Formula: C11H10N2OS
• Molecular Weight: 218.2749
• MDL Number: MFCD01314303
• SMILES: NC(=O)c1cc(sc1N)c1ccccc1

Computed Properties

• Complexity: 241
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 15
• Hydrogen Bond Acceptor Count: 3
• Hydrogen Bond Donor Count: 2
• Rotatable Bond Count: 2
• XLogP3: 2.3

Upstream Synthesis Route

2-Amino-5-phenylthiophene-3-carboxamide, also known as $name$, is a versatile compound widely used in chemical synthesis. Its unique structure makes it a valuable building block for the creation of various organic compounds. In particular, $name$ is commonly employed as a key intermediate in the synthesis of pharmaceuticals, agrochemicals, and functional materials.One of the key applications of 2-Amino-5-phenylthiophene-3-carboxamide in chemical synthesis is its role as a precursor in the development of novel medications. By incorporating this compound into the synthesis of pharmaceutical agents, researchers can modify the properties and biological activities of the resulting drugs. Additionally, $name$ can be utilized in the production of agrochemicals, where its structure contributes to the enhancement of pesticide or herbicide potency.Furthermore, 2-Amino-5-phenylthiophene-3-carboxamide finds importance in the synthesis of functional materials such as polymers and dyes. Its presence in the chemical reaction pathways imparts desirable characteristics to the final products, leading to the creation of materials with specific properties and applications.Overall, the versatile nature of $name$ makes it a valuable tool in the realm of chemical synthesis, enabling the development of innovative compounds with diverse practical uses.

Literature

• Synthesis and SAR studies of 1,4-benzoxazine MenB inhibitors: novel antibacterial agents against Mycobacterium tuberculosis.

  Bioorganic & medicinal chemistry letters 20101101