Description

7-Oxabicyclo[4.1.0]Heptan-2-Ol,4-(1-Methylethyl)-,(1R,2R,4S,6S)-Rel-(9Ci) is a high-purity, stereochemically defined oxabicyclic compound that serves as a critical chiral building block and intermediate in advanced organic synthesis. Its rigid, functionalized bicyclic structure makes it a valuable precursor for developing complex molecules with specific three-dimensional architectures. This compound is primarily sought by research institutions and manufacturers in the pharmaceutical and agrochemical sectors for applications in asymmetric synthesis, medicinal chemistry, and the development of novel active ingredients.

Application

• Pharmaceutical Intermediate: A key chiral synthon for the research and development of new active pharmaceutical ingredients (APIs), particularly in areas requiring stereochemical control.
• Agrochemical Synthesis: Used in the production of advanced crop protection agents and pesticides where its specific stereochemistry can influence biological activity.
• Asymmetric Catalysis: Serves as a precursor or ligand in the development of chiral catalysts for enantioselective reactions.
• Medicinal Chemistry Research: Employed in drug discovery programs to construct complex, polycyclic molecular scaffolds for biological screening.
• Fine Chemical Production: Utilized in the multi-step synthesis of specialty chemicals, flavors, and fragrances requiring high stereopurity.
• Academic & Industrial R&D: A valuable tool for synthetic organic chemists exploring new reaction methodologies and natural product synthesis.

Basic Information

Product Name	7-Oxabicyclo[4.1.0]Heptan-2-Ol,4-(1-Methylethyl)-,(1R,2R,4S,6S)-Rel-(9Ci)
CAS No.	217310-18-4
Molecular Formula	C9H16O2
Molecular Weight	156.22 g/mol
Synonyms	(1R,2R,4S,6S)-rel-4-Isopropyl-7-oxabicyclo[4.1.0]heptan-2-ol; 4-Isopropyl-7-oxabicyclo[4.1.0]heptan-2-ol, (1R,2R,4S,6S)-rel-; rel-(1R,2R,4S,6S)-4-(1-Methylethyl)-7-oxabicyclo[4.1.0]heptan-2-ol; Oxabicycloheptanol derivative; Chiral Oxabicyclic Alcohol; Bicyclic Ether Alcohol Intermediate
EINECS	Contact for details

Quality Control

We maintain stringent quality control protocols for our chiral intermediates. Production adheres to current Good Manufacturing Practices (cGMP) where applicable, ensuring batch-to-batch consistency and traceability. Quality is verified through comprehensive analytical techniques including chiral HPLC, GC, NMR, and optical rotation measurement to confirm identity, purity, and enantiomeric excess. A detailed Certificate of Analysis (COA) is provided with each shipment, and specifications can be aligned with client-specific requirements.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, and well-ventilated area at a controlled room temperature (typically 15-25°C). The container should be kept tightly sealed to protect against moisture. Keep away from heat, sparks, and open flame.

Specification

Item	Specification
Appearance	White to off-white crystalline powder or solid
Identification (IR)	Conforms to structure
Identification (NMR)	Conforms to structure
Purity (HPLC)	≥ 98.0%
Enantiomeric Excess (Chiral HPLC)	≥ 99.0%
Optical Rotation	Contact for details
Loss on Drying	≤ 0.5%
Residue on Ignition	≤ 0.1%

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