Description

Oxiranemethanol,2-Methyl-3-[(Phenylmethoxy)Methyl]-,(2R,3R)-Rel-(9Ci) is a high-purity, stereochemically defined chiral epoxide building block of significant synthetic utility. This compound matters as a versatile intermediate for the precise construction of complex molecules, enabling the synthesis of enantiomerically pure pharmaceuticals and fine chemicals. It is primarily needed by research and development chemists and process development teams in the pharmaceutical, agrochemical, and advanced materials industries.

Application

• Pharmaceutical Intermediate: Key chiral synthon for the synthesis of active pharmaceutical ingredients (APIs), particularly in routes requiring stereospecific ring-opening reactions.
• Agrochemical Synthesis: Used in the research and production of enantiomerically pure herbicides, fungicides, and plant growth regulators.
• Asymmetric Catalysis Research: Serves as a standard substrate or ligand precursor in the development and screening of new chiral catalysts.
• Fine Chemical Production: Enables the manufacture of specialty chemicals, flavors, and fragrances where specific stereochemistry is critical for function.
• Material Science: Potential monomer or cross-linking agent in the development of advanced polymers with tailored properties.
• Academic & Contract Research: Essential reagent for methodological studies in organic synthesis and medicinal chemistry within academic and CRO (Contract Research Organization) settings.

Basic Information

Product Name	Oxiranemethanol,2-Methyl-3-[(Phenylmethoxy)Methyl]-,(2R,3R)-Rel-(9Ci)
CAS No.	794513-02-3
Molecular Formula	C12H16O3
Molecular Weight	208.25 g/mol
Synonyms	(2R,3R)-2-Methyl-3-(benzyloxymethyl)oxiranemethanol; rel-(2R,3R)-2-Methyl-3-[(phenylmethoxy)methyl]oxiranemethanol; (2R,3R)-2-Methyl-3-(benzyloxymethyl)glycidol; Benzyl (2R,3R)-2-methyl-3-(hydroxymethyl)oxiranylmethyl ether; Glycidol, 2-methyl-3-(benzyloxymethyl)-, (2R,3R)-rel-; Chiral Benzyl-Protected Glycidol Derivative
EINECS	Contact for details

Quality Control

Our production of this chiral building block adheres to strict quality protocols to ensure batch-to-batch consistency and high enantiomeric purity. Each lot is supported by a comprehensive Certificate of Analysis (COA) detailing identity, purity (HPLC/GC), chiral purity, and impurity profiles. We employ advanced analytical techniques including Chiral HPLC, NMR, and IR spectroscopy for verification. Quality standards are designed to meet the rigorous demands of GMP-guided synthesis and research applications.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry place at a controlled room temperature (15-25°C). This product is hygroscopic (moisture-sensitive); ensure the container is sealed under an inert atmosphere after each use to maintain stability and prevent degradation.

Specification

Item	Specification
Appearance	Colorless to pale yellow liquid
Identification (IR)	Conforms to structure
Purity (HPLC)	≥ 97.0%
Chiral Purity (Chiral HPLC)	≥ 99.0% ee (2R,3R)
Water Content (KF)	≤ 0.5%

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