Description

(S)-1-(2,6-Dichloro-3-Fluorophenyl)Ethanol is a high-purity chiral intermediate of significant importance in modern pharmaceutical synthesis. Its value lies in its role as a key building block for constructing complex, biologically active molecules with defined stereochemistry. This compound is primarily needed by research institutions and manufacturers in the pharmaceutical and agrochemical industries for the development of new active ingredients.

Application

• Pharmaceutical Intermediate: A critical chiral synthon for the research and production of novel active pharmaceutical ingredients (APIs), particularly in therapeutic areas requiring high stereochemical purity.
• Agrochemical Synthesis: Used in the development of advanced pesticides and herbicides where the specific (S)-enantiomer imparts desired biological activity.
• Asymmetric Catalysis Research: Serves as a valuable substrate or ligand precursor in academic and industrial research focused on developing new chiral catalysts and synthetic methodologies.
• Fine Chemical Production: Employed in the multi-step synthesis of other specialized fine chemicals and complex organic molecules for various high-tech applications.
• Reference Standard: Used as an analytical standard in quality control laboratories for method development and validation in chiral separation techniques like HPLC.

Basic Information

Product Name	(S)-1-(2,6-Dichloro-3-Fluorophenyl)Ethanol
CAS No.	877397-65-4
Molecular Formula	C8H7Cl2FO
Molecular Weight	209.05 g/mol
Synonyms	(S)-1-(2,6-Dichloro-3-fluorophenyl)ethan-1-ol; (S)-α-(2,6-Dichloro-3-fluorophenyl)ethanol; (S)-2,6-Dichloro-3-fluoro-α-methylbenzyl alcohol; (1S)-1-(2,6-Dichloro-3-fluorophenyl)ethanol; (S)-(-)-1-(2,6-Dichloro-3-fluorophenyl)ethanol; (S)-1-(2,6-Dichloro-3-fluorophenyl)ethyl alcohol
EINECS	Contact for details

Quality Control

Our (S)-1-(2,6-Dichloro-3-Fluorophenyl)Ethanol is manufactured under strict quality management systems. Every batch undergoes rigorous analytical testing, including chiral purity determination by HPLC, to ensure it meets the high standards required for pharmaceutical R&D and production. A comprehensive Certificate of Analysis (COA) detailing identity, purity, and impurity profiles is provided with each shipment.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, and well-ventilated place at a controlled room temperature (typically 15-25°C). Keep away from strong oxidizing agents.

Specification

Item	Specification
Appearance	White to off-white crystalline powder
Identification (IR)	Conforms to structure
Assay (HPLC)	≥ 98.0%
Chiral Purity (HPLC)	≥ 99.0% ee
Related Substances (HPLC)	Total impurities ≤ 2.0%
Residual Solvents (GC)	Meets ICH guidelines

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