1001020-13-8 | (3-Trifluoromethyl-1h-pyrazol-4-yl)methanol

Packsize	Purity	Availability	Price	Discounted Price
100mg	97%	in stock	$13.00	$10.00
250mg	97%	in stock	$27.00	$19.00

Description

• Catalog Number: AA01049
• Chemical Name: (3-Trifluoromethyl-1h-pyrazol-4-yl)methanol
• CAS Number: 1001020-13-8
• Molecular Formula: C5H5F3N2O
• Molecular Weight: 166.10120959999995
• MDL Number: MFCD16620670
• SMILES: OCc1c[nH]nc1C(F)(F)F

Computed Properties

• Complexity: 138
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 11
• Hydrogen Bond Acceptor Count: 5
• Hydrogen Bond Donor Count: 2
• Rotatable Bond Count: 1
• XLogP3: 0.2

Upstream Synthesis Route

The compound (3-Trifluoromethyl-1H-pyrazol-4-yl)methanol is a versatile building block in chemical synthesis, particularly valued for its ability to introduce a trifluoromethyl group into organic molecules. This functionality is highly sought after in medicinal chemistry, agrochemicals, and materials science due to the unique electronic and steric properties that the trifluoromethyl group imparts. In organic synthesis, (3-Trifluoromethyl-1H-pyrazol-4-yl)methanol can be used as a key starting material for the construction of various biologically active compounds, pharmaceuticals, and crop protection agents. Its presence can enhance the biological activity, metabolic stability, and lipophilicity of the final products, making it a valuable tool for drug discovery and development. Moreover, the trifluoromethyl group in (3-Trifluoromethyl-1H-pyrazol-4-yl)methanol can also serve as a synthetic handle for further derivatization, allowing for the modification and optimization of the molecular properties of the target molecules. This compound's role in chemical synthesis extends beyond organic chemistry, playing a vital part in the creation of advanced materials and functional polymers with tailored properties.Overall, (3-Trifluoromethyl-1H-pyrazol-4-yl)methanol is a crucial building block with diverse applications in chemical synthesis, enabling the efficient and precise introduction of trifluoromethyl functionality into a wide range of compounds with significant potential in pharmaceutical, agricultural, and materials research.