1119489-35-8 | 1-(3-Fluorophenyl)-5-(trifluoromethyl)-1H-pyrazole-4-carboxylic acid

Packsize	Purity	Availability	Price	Discounted Price
50mg	95%	1 week	$112.00	$79.00
100mg	95%	1 week	$142.00	$100.00
250mg	95%	1 week	$181.00	$127.00
500mg	95%	1 week	$258.00	$181.00
1g	95%	1 week	$315.00	$221.00
2.5g	95%	1 week	$608.00	$426.00
5g	95%	1 week	$1,153.00	$807.00
10g	95%	1 week	$2,199.00	$1,540.00

Description

• Catalog Number: AW40056
• Chemical Name: 1-(3-Fluorophenyl)-5-(trifluoromethyl)-1H-pyrazole-4-carboxylic acid
• CAS Number: 1119489-35-8
• Molecular Formula: C11H6F4N2O2
• Molecular Weight: 274.1712
• MDL Number: MFCD16418002
• SMILES: Fc1cccc(c1)n1ncc(c1C(F)(F)F)C(=O)O

Computed Properties

• Complexity: 350
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 19
• Hydrogen Bond Acceptor Count: 7
• Hydrogen Bond Donor Count: 1
• Rotatable Bond Count: 2
• XLogP3: 2.4

Upstream Synthesis Route

1-(3-fluorophenyl)-5-(trifluoromethyl)-1H-pyrazole-4-carboxylic acid, also known as $name$, plays a significant role in chemical synthesis as a versatile building block. This compound is commonly utilized as a key intermediate in the preparation of organic molecules with diverse functionalities.In the realm of chemical synthesis, $name$ serves as a crucial starting material for the construction of various biologically active compounds, pharmaceuticals, and agrochemicals. Its unique structure containing both fluorine and phenyl moieties imparts specific properties that are valuable in designing new chemical entities with desirable characteristics.Researchers and chemists frequently employ $name$ in the creation of novel heterocyclic compounds through multistep synthesis routes. Its trifluoromethyl and fluorophenyl groups offer opportunities for introducing steric hindrance, electron density, and lipophilicity into the target molecules, thereby influencing their biological activities and pharmacokinetic profiles.Moreover, due to the presence of a carboxylic acid functional group, $name$ can participate in various chemical transformations such as amidation, esterification, and cross-coupling reactions. This feature enables further diversification of its chemical structure, leading to the synthesis of a wide range of complex organic molecules with tailored properties.In summary, the application of 1-(3-fluorophenyl)-5-(trifluoromethyl)-1H-pyrazole-4-carboxylic acid in chemical synthesis extends beyond being just a building block - it serves as a crucial tool for the creation of intricate and functional molecules with potential applications in medicinal chemistry, materials science, and other fields requiring advanced organic synthesis techniques.