Description

3-(Methylsulfonyl)-6-Oxa-3-Azabicyclo[3.1.0]Hexane is a high-purity, advanced pharmaceutical intermediate featuring a unique bridged bicyclic structure. This compound is of significant commercial importance as a key building block in the synthesis of complex active pharmaceutical ingredients (APIs), particularly those targeting central nervous system disorders. It is primarily sought after by research institutions and manufacturers in the global pharmaceutical and agrochemical industries for developing novel therapeutic agents and crop protection products.

Application

• Pharmaceutical Intermediate: A critical precursor in the synthesis of novel drug candidates, especially for neurological targets.
• Agrochemical Synthesis: Used as a building block for developing advanced pesticides and herbicides with specific modes of action.
• Chemical Research: Serves as a versatile scaffold in medicinal chemistry for structure-activity relationship (SAR) studies and library synthesis.
• Process Development: Employed in scaling up synthetic routes for pilot and commercial-scale API manufacturing.
• Custom Synthesis: A starting material for contract research organizations (CROs) and CDMOs producing specialized compounds for clients.

Basic Information

Product Name	3-(Methylsulfonyl)-6-Oxa-3-Azabicyclo[3.1.0]Hexane
CAS No.	185423-66-9
Molecular Formula	C7H11NO3S
Molecular Weight	189.23 g/mol
Synonyms	6-Oxa-3-azabicyclo[3.1.0]hexane, 3-(methylsulfonyl)-; 3-(Methylsulfonyl)-6-oxa-3-azabicyclo[3.1.0]hexane; 3-Methanesulfonyl-6-oxa-3-azabicyclo[3.1.0]hexane; 3-Methylsulfonyl-6-oxa-3-azabicyclo[3.1.0]hexane; (1R,5S)-3-(Methylsulfonyl)-6-oxa-3-azabicyclo[3.1.0]hexane; (1S,5R)-3-(Methylsulfonyl)-6-oxa-3-azabicyclo[3.1.0]hexane
EINECS	Contact for details

Quality Control

Our production of 3-(Methylsulfonyl)-6-Oxa-3-Azabicyclo[3.1.0]Hexane adheres to stringent quality management protocols to ensure batch-to-batch consistency and high purity. All material is released with a comprehensive Certificate of Analysis (COA) detailing key parameters such as assay, identity, and impurity profiles. We support customer audits and can provide material manufactured under cGMP guidelines for advanced pharmaceutical applications upon request.

Storage

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

Specification

Item	Specification
Appearance	White to off-white crystalline powder
Identification (IR)	Conforms to structure
Assay (HPLC)	≥ 98.0%
Related Substances (HPLC)	Total impurities ≤ 2.0%
Any single unknown impurity	≤ 0.5%
Residual Solvents (GC)	Meets ICH Q3C guidelines
Water Content (KF)	≤ 0.5%

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