Description

3-Cyclohexen-1-Ol,2-Ethyl-5,6-Bis(Methoxymethyl)-,(1R,2S,5S,6R)-Rel-(9Ci) is a high-purity, stereochemically defined chiral intermediate of significant interest in advanced organic synthesis. Its complex, functionalized cyclohexene structure makes it a valuable building block for constructing intricate molecular architectures with precise spatial orientation. This compound is primarily sought after by research and development teams in the pharmaceutical and agrochemical sectors for the synthesis of novel active ingredients and fine chemicals.

Application

• Pharmaceutical Intermediate: A key chiral synthon for the research and development of new drug candidates, particularly in areas requiring complex, multi-functionalized ring systems.
• Agrochemical Synthesis: Used in the creation of advanced, stereospecific pesticides, herbicides, and plant growth regulators.
• Advanced Material Research: Serves as a precursor in the development of specialty polymers, liquid crystals, or organic electronic materials requiring specific molecular geometries.
• Asymmetric Catalysis: Employed as a ligand precursor or a test substrate in the development and optimization of new asymmetric catalytic processes.
• Academic & Industrial R&D: A valuable tool for synthetic organic chemists in universities and corporate labs exploring new reaction methodologies and complex natural product synthesis.

Basic Information

Product Name	3-Cyclohexen-1-Ol,2-Ethyl-5,6-Bis(Methoxymethyl)-,(1R,2S,5S,6R)-Rel-(9Ci)
CAS No.	522603-79-8
Molecular Formula	C13H24O3
Molecular Weight	228.33 g/mol
Synonyms	(1R,2S,5S,6R)-rel-2-Ethyl-5,6-bis(methoxymethyl)cyclohex-3-en-1-ol; rel-(1R,2S,5S,6R)-2-Ethyl-5,6-bis(methoxymethyl)-3-cyclohexen-1-ol; 2-Ethyl-5,6-bis(methoxymethyl)cyclohex-3-en-1-ol (relative stereochemistry); Chiral Cyclohexenol Derivative; Functionalized Chiral Cyclohexene
EINECS	Contact for details

Quality Control

Our production of this advanced chiral intermediate adheres to strict quality management protocols. Every batch is characterized using advanced analytical techniques including Chiral HPLC, GC, and NMR to ensure stereochemical purity and chemical identity. A comprehensive Certificate of Analysis (COA) detailing purity, enantiomeric excess, and impurity profiles is provided with each shipment to support your critical R&D and scale-up activities.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry place at a controlled room temperature (typically 15-25°C). Keep the container sealed under an inert atmosphere if long-term storage is required to maintain optimal purity.

Specification

Item	Specification
Appearance	Colorless to pale yellow liquid
Identification (IR)	Conforms to structure
Identification (NMR)	Conforms to structure
Purity (GC/HPLC)	≥ 95.0% (Area %)
Enantiomeric Excess (Chiral HPLC)	≥ 99.0% e.e.
Water Content (KF)	≤ 0.5%

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