Description

(S)-1-Chlorohept-6-En-2-Ol is a chiral, halogenated alcohol building block of significant interest in advanced organic synthesis. Its unique structure, featuring both a terminal alkene and a chlorinated alcohol moiety, makes it a versatile precursor for constructing complex, optically active molecules. This compound is primarily utilized by research chemists and process development scientists in the pharmaceutical and agrochemical industries for applications such as asymmetric synthesis and the development of novel active ingredients.

Application

• Pharmaceutical Intermediate: A key chiral synthon for the synthesis of potential drug candidates, particularly in the development of antiviral, anti-inflammatory, or central nervous system (CNS) active compounds.
• Agrochemical Synthesis: Used in the research and production of chiral pesticides, herbicides, and fungicides where specific stereochemistry is crucial for bioactivity.
• Ligand and Catalyst Development: Serves as a precursor for synthesizing chiral ligands and organocatalysts used in asymmetric catalysis.
• Fine Chemical Production: Employed in the manufacture of specialty chemicals, flavors, and fragrances requiring high enantiomeric purity.
• Academic and R&D: A valuable tool in academic research for methodological studies in stereoselective halogenation, olefin functionalization, and cross-coupling reactions.
• Material Science Precursor: Can be utilized to introduce functional groups into polymers or dendrimers for advanced material applications.

Basic Information

Product Name	(S)-1-Chlorohept-6-En-2-Ol
CAS No.	1224174-07-5
Molecular Formula	C7H13ClO
Molecular Weight	148.63 g/mol
Synonyms	(S)-6-Hepten-2-ol, 1-chloro-; (2S)-1-Chloro-6-hepten-2-ol; (S)-1-Chloro-6-hepten-2-ol; 1-Chloro-6-hepten-2-ol, (S)-; (S)-1-Chlorohept-6-en-2-ol; (S)-1-Chloro-6-heptene-2-ol; (2S)-1-Chlorohept-6-en-2-ol
EINECS	Contact for details

Quality Control

Our (S)-1-Chlorohept-6-En-2-Ol is produced under strict quality management protocols. Each batch is characterized and tested to ensure identity, purity, and enantiomeric excess meet the high standards required for research and development. A comprehensive Certificate of Analysis (COA) is provided with each shipment, detailing results for key parameters such as assay (by GC/HPLC), enantiomeric purity (by chiral HPLC), and identification (by IR/NMR).

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, well-ventilated place at a controlled room temperature (typically 15-25°C). Keep away from heat, sparks, and open flame. Due to the light-sensitive nature of the compound, containers should be amber glass or otherwise opaque.

Specification

Item	Specification
Appearance	Colorless to pale yellow liquid
Identification (IR)	Conforms to structure
Purity (GC/HPLC)	≥ 97.0%
Enantiomeric Excess (Chiral HPLC)	≥ 98.0%
Water Content (KF)	≤ 0.5%

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