1047630-55-6 | 5-Chloro-4-(1-methyl-1H-pyrazol-5-yl)thiophene-2-carboxylic acid

Packsize	Purity	Availability	Price	Discounted Price
1mg		2 weeks	$105.00	$73.00
2mg		2 weeks	$123.00	$86.00
3mg		2 weeks	$149.00	$105.00
5mg		2 weeks	$168.00	$118.00
10mg		2 weeks	$193.00	$135.00

Description

• Catalog Number: AV18858
• Chemical Name: 5-Chloro-4-(1-methyl-1H-pyrazol-5-yl)thiophene-2-carboxylic acid
• CAS Number: 1047630-55-6
• Molecular Formula: C9H7ClN2O2S
• Molecular Weight: 242.6821
• MDL Number: MFCD30489217
• SMILES: Clc1sc(cc1c1ccnn1C)C(=O)O

Computed Properties

• Complexity: 267
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 15
• Hydrogen Bond Acceptor Count: 4
• Hydrogen Bond Donor Count: 1
• Rotatable Bond Count: 2
• XLogP3: 2.4

Upstream Synthesis Route

In the field of chemical synthesis, 5-Chloro-4-(1-methyl-1H-pyrazol-5-yl)-2-thiophenecarboxylic acid serves as a valuable building block for the creation of novel compounds with potential pharmaceutical and agrochemical applications. This specific compound plays a crucial role as a versatile intermediate in the synthesis of various heterocyclic molecules with diverse properties and functionalities. By incorporating this compound into synthetic pathways, chemists can access a wide range of structurally complex compounds that exhibit unique biological activities and interactions.The presence of the chloro, methylpyrazole, and thiophene functional groups in 5-Chloro-4-(1-methyl-1H-pyrazol-5-yl)-2-thiophenecarboxylic acid imparts it with distinctive reactivity and selectivity in chemical transformations. Through targeted modifications and derivatizations of these functional groups, researchers can tailor the properties of the resulting compounds for specific applications in drug discovery, material science, and other relevant fields. Additionally, the strategic positioning of these functional groups enables precise control over the stereochemistry and regiochemistry of the synthesized molecules, allowing for the creation of complex molecular architectures with high precision and efficiency.Furthermore, the unique structural features of 5-Chloro-4-(1-methyl-1H-pyrazol-5-yl)-2-thiophenecarboxylic acid make it an attractive substrate for the development of innovative synthetic methodologies and strategies. Its versatile nature and synthetic accessibility provide chemists with a powerful tool for exploring new chemical reactions, cascade processes, and multicomponent reactions to streamline the synthesis of complex compounds and accelerate the discovery of bioactive molecules with therapeutic potential. By harnessing the synthetic utility of this key intermediate, researchers can unlock new opportunities for advancing the frontiers of chemical synthesis and expanding the scope of molecular diversity for various applications.