Description

2,6-Dioxabicyclo[3.1.0]Hex-3-Ene-1-Methanol is a specialized bicyclic oxirane derivative, a high-value synthetic intermediate prized for its unique strained-ring structure and functional group versatility. This compound matters for its role as a critical building block in the synthesis of complex molecules, enabling the introduction of chiral centers and oxygenated functionalities. It is primarily needed by research and development chemists in the pharmaceutical and agrochemical industries for creating novel active ingredients and fine chemicals.

Application

• Pharmaceutical Intermediate: A key chiral synthon for the development of novel active pharmaceutical ingredients (APIs), particularly in antiviral, anticancer, and anti-inflammatory drug discovery programs.
• Agrochemical Synthesis: Used in the research and production of advanced pesticides and herbicides, where its bicyclic structure can contribute to unique biological activity.
• Material Science Research: Serves as a monomer or cross-linking agent in the development of specialty polymers and resins with tailored thermal or mechanical properties.
• Asymmetric Catalysis: Employed as a ligand precursor or a substrate in asymmetric synthesis to construct complex, enantiomerically pure molecules.
• Fine Chemical Production: Acts as a versatile intermediate for synthesizing flavors, fragrances, and other high-value specialty chemicals.

Basic Information

Product Name	2,6-Dioxabicyclo[3.1.0]Hex-3-Ene-1-Methanol
CAS No.	860383-07-9
Molecular Formula	C6H8O3
Molecular Weight	128.13 g/mol
Synonyms	1-(Hydroxymethyl)-2,6-dioxabicyclo[3.1.0]hex-3-ene; 2,6-Dioxabicyclo[3.1.0]hex-3-ene-1-methanol; Bicyclic Oxirane Methanol Derivative; 3-Oxa-7-oxabicyclo[4.1.0]hept-4-ene-1-methanol; (1R,5S,6S)-6-(Hydroxymethyl)-3-oxa-7-oxabicyclo[4.1.0]hept-4-ene (enantiomer); (1S,5R,6R)-6-(Hydroxymethyl)-3-oxa-7-oxabicyclo[4.1.0]hept-4-ene (enantiomer)
EINECS	Contact for details

Quality Control

Our 2,6-Dioxabicyclo[3.1.0]Hex-3-Ene-1-Methanol is produced under strict quality management systems. Each batch undergoes rigorous analytical testing, including chiral purity analysis, to ensure it meets the exacting standards required for advanced synthetic applications. Certificates of Analysis (COA) detailing identity, purity, and impurity profiles are available upon request to support your quality assurance and regulatory needs.

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). This compound may be sensitive to moisture and prolonged exposure to air; keep the container tightly sealed under an inert atmosphere if specified.

Specification

Item	Specification
Appearance	Colorless to pale yellow liquid or low-melting solid
Identification (IR)	Conforms to structure
Purity (HPLC)	≥ 97.0%
Chiral Purity (Chiral HPLC)	≥ 98.0% ee (for enantiomerically enriched grades)
Water Content (KF)	≤ 0.5%

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