1134-50-5 | 1-Phenyl-1h-pyrazole-4-carboxylic acid

Packsize	Purity	Availability	Price	Discounted Price
1g	98%	in stock	$33.00	$24.00
5g	98%	in stock	$81.00	$57.00
10g	98%	in stock	$162.00	$114.00
25g	98%	in stock	$368.00	$258.00

Description

• Catalog Number: AA10743
• Chemical Name: 1-Phenyl-1h-pyrazole-4-carboxylic acid
• CAS Number: 1134-50-5
• Molecular Formula: C10H8N2O2
• Molecular Weight: 188.1827
• MDL Number: MFCD00514518
• SMILES: OC(=O)c1cnn(c1)c1ccccc1

Computed Properties

• Complexity: 214
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 14
• Hydrogen Bond Acceptor Count: 3
• Hydrogen Bond Donor Count: 1
• Rotatable Bond Count: 2
• XLogP3: 1.4

Upstream Synthesis Route

1-Phenyl-1H-pyrazole-4-carboxylic acid, also known as $name$, plays a crucial role in chemical synthesis as a versatile building block. This compound is widely utilized in the pharmaceutical industry for the synthesis of various bioactive molecules and pharmaceutical agents. Its unique chemical properties make it an essential component in the development of innovative drugs and therapeutic compounds.$name$ is frequently employed as a key intermediate in the preparation of heterocyclic compounds with diverse biological activities. Its functional groups enable it to participate in a wide range of chemical reactions, including coupling reactions, acylation, and cyclization processes. By incorporating $name$ into organic synthesis pathways, chemists can efficiently access structurally complex molecules with potential pharmacological properties.In addition to its pharmaceutical applications, $name$ serves as a valuable building block in the synthesis of agrochemicals, dyes, and advanced materials. Its compatibility with various synthetic methodologies and its ability to introduce functional groups make it a versatile tool for organic chemists seeking to create new molecules with specific properties.Overall, the application of 1-Phenyl-1H-pyrazole-4-carboxylic acid in chemical synthesis is instrumental in the development of novel compounds for pharmaceutical, agricultural, and materials science purposes. Its versatility and reactivity make it a valuable asset in the toolkit of synthetic chemists aiming to drive innovation in diverse fields.

Literature

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

  Bioorganic & medicinal chemistry letters 20101101