Description

(3-(2,4-Dichlorophenyl)-1-(2-Fluorophenyl)-1H-Pyrazol-4-Yl)Methanol is a high-purity, advanced pharmaceutical intermediate designed for the synthesis of complex active ingredients. This compound is critical for research and development in medicinal chemistry, offering a versatile pyrazole-based scaffold for creating novel therapeutic agents. It is primarily utilized by pharmaceutical manufacturers and R&D laboratories focused on developing new drug candidates, particularly in areas requiring sophisticated heterocyclic chemistry.

Application

• Pharmaceutical Intermediate: Serves as a key building block in the synthesis of novel active pharmaceutical ingredients (APIs) and drug candidates.
• Medicinal Chemistry Research: Used in structure-activity relationship (SAR) studies and lead optimization for new therapeutic targets.
• Agrochemical Development: Acts as a precursor in the research and synthesis of new-generation pesticides and herbicides.
• Chemical Synthesis: Employed as a versatile intermediate for constructing complex molecules in organic and process chemistry.
• Biochemical Research: Utilized in the development of enzyme inhibitors and other bioactive compounds.

Basic Information

Product Name	(3-(2,4-Dichlorophenyl)-1-(2-Fluorophenyl)-1H-Pyrazol-4-Yl)Methanol
CAS No.	618444-51-2
Molecular Formula	C16H11Cl2FN2O
Molecular Weight	337.18 g/mol
Synonyms	4-(Hydroxymethyl)-1-(2-fluorophenyl)-3-(2,4-dichlorophenyl)-1H-pyrazole; 1-(2-Fluorophenyl)-3-(2,4-dichlorophenyl)-1H-pyrazole-4-methanol; 618444-51-2; (3-(2,4-Dichlorophenyl)-1-(2-fluorophenyl)-1H-pyrazol-4-yl)methanol; Pyrazole-4-methanol derivative; Fluorophenyl dichlorophenyl pyrazole methanol
EINECS	Contact for details

Quality Control

Our (3-(2,4-Dichlorophenyl)-1-(2-Fluorophenyl)-1H-Pyrazol-4-Yl)Methanol is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing, including HPLC, NMR, and mass spectrometry, to ensure identity, purity, and consistency. Certificates of Analysis (COA) are provided with every shipment, detailing all relevant specifications. We adhere to cGMP principles where applicable to support our clients in regulated pharmaceutical development.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, well-ventilated area at a controlled room temperature (15-25°C). Keep away from strong oxidizing agents and incompatible materials. For long-term storage, consider an inert atmosphere to maintain product integrity.

Specification

Item	Specification
Appearance	White to off-white crystalline powder
Identification (IR)	Conforms to structure
Identification (HPLC)	Conforms to reference standard
Assay (HPLC)	≥ 98.0%
Related Substances (HPLC)	Total impurities ≤ 2.0%
Any single impurity	≤ 0.5%
Loss on Drying	≤ 0.5%
Residue on Ignition	≤ 0.1%

Note: Specifications can be tailored. Please contact us for the detailed technical data sheet of a specific grade.