(3aR,6S,6aR)-6-(((tert-butyldiphenylsilyl)oxy)methyl)-2,2-dimethyldihydrofuro[3,4-d][1,3]dioxol-4(3aH)-one | CAS 1320269-76-8

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  • Availability: Lead time 4-6 weeks
  • Catalogue number: RM-D-427
  • Synonyms: (3aR,6S,6aR)-6-(TBDPSO-methyl)-2,2-dimethyldihydrofuro[3,4-d][1,3]dioxol-4(3aH)-one
  • Price Match Policy: We match verified competitor quote prices.
SKU: RM-D-427 Category:

PRODUCT NAME

(3aR,6S,6aR)-6-(((tert-butyldiphenylsilyl)oxy)methyl)-2,2-dimethyldihydrofuro[3,4-d][1,3]dioxol-4(3aH)-one

CAS Number: 1320269-76-8


SYNONYMS & IDENTIFIERS

  • (3aR,6S,6aR)-6-(((tert-butyldiphenylsilyl)oxy)methyl)-2,2-dimethyldihydrofuro[3,4-d][1,3]dioxol-4(3aH)-one

  • Protected dioxolane-furanone intermediate

  • Silyl ether functional intermediate

  • CAS: 1320269-76-8


CHEMICAL STRUCTURE & FORMULA

  • Molecular Formula: Câ‚‚â‚‚H₂₈Oâ‚…Si

  • Molecular Weight: 396.52 g/mol

  • Structure Type: Fused bicyclic lactone with a tert-butyldiphenylsilyl (TBDPS) protecting group

This compound features a protected hydroxymethyl group (tert-butyldiphenylsilyl ether) attached to a bicyclic dihydrofuro[3,4-d][1,3]dioxol-4-one core. The configuration at the stereocenters is specified as (3aR,6S,6aR), indicating defined spatial relationships critical for downstream transformations.


KEY FEATURES & BENEFITS

 

HIGH-PURITY PROTECTED SYNTHETIC INTERMEDIATE

This compound is manufactured to high purity standards suitable for complex organic synthesis, medicinal chemistry, and process research. The TBDPS protecting group offers enhanced stability under a variety of reaction conditions.

STEREOCHEMICAL DEFINITENESS

The defined stereochemistry (3aR,6S,6aR) ensures reliable behavior in stereospecific transformations, a crucial requirement for synthesis of advanced chiral targets.

VERSATILE FUNCTIONALITY

Featuring both a bicyclic lactone system and a masked hydroxymethyl group, this intermediate can serve as a key building block in multistep syntheses — particularly where controlled deprotection and ring-opening sequences are needed.

SUITABLE FOR SCALE-UP

Our quality control and batch testing ensure that this product performs consistently from milligram to multi-gram scale reactions, supporting both discovery chemistry and early process development.


APPLICATIONS  of  (3aR,6S,6aR)-6-(((tert-butyldiphenylsilyl)oxy)methyl)-2,2-dimethyldihydrofuro[3,4-d][1,3]dioxol-4(3aH)-one | CAS 1320269-76-8

 

The compound is ideally positioned for use in a range of synthetic and pharmaceutical research applications:

MEDICINAL CHEMISTRY

  • As a chiral intermediate in the construction of heterocyclic frameworks

  • For design and optimization of small molecules with biological activity

  • In structure-activity relationship (SAR) studies requiring stereodefined intermediates

TOTAL SYNTHESIS

  • Useful in complex natural product synthesis where protected hydroxymethyl groups and bicyclic lactone cores are required

  • Facilitates sequential functional group manipulations with minimized side reactions

PROTECTING GROUP STRATEGIES

The TBDPS group provides:

  • High resistance to basic and mildly acidic conditions

  • Selective removal with fluoride sources (e.g., TBAF) when required

  • Compatibility with multi-step synthetic workflows

PROCESS RESEARCH & DEVELOPMENT

  • Evaluation in scale-up strategies

  • Optimization of deprotection and functionalization sequences

  • Assessment of reagent compatibility and step-economy


SYNTHETIC UTILITY & REACTIVITY CHARACTERISTICS

TBDPS PROTECTION

The tert-butyldiphenylsilyl (TBDPS) group is chosen for its:

  • Exceptional stability relative to other silyl protecting groups (e.g., TMS, TBDMS)

  • Resistance to hydrolysis and migration under a broad range of conditions

  • Ability to selectively protect primary alcohol functionality

DIHYDROFURO[3,4-D][1,3]DIOXOL-4(3AH)-ONE CORE

This bicyclic system imparts:

  • A rigid framework that can influence downstream stereochemistry

  • A lactone handle for ring-opening, nucleophilic attack, or reduction

  • Opportunities for diversification via functional group interconversion


ANALYTICAL CHARACTERISTICS & QUALITY ASSURANCE

ResolveMass adheres to strict quality protocols, delivering material with:

  • Purity: Verified by HPLC and/or NMR analysis

  • Identity Confirmation: Assessed via NMR, MS, and, where applicable, IR spectroscopy

  • Batch Consistency: Synthetic reproducibility ensures consistent performance

  • Documentation: Commercial batches include a Certificate of Analysis (CoA)

Analytical data and CoA are provided upon request to support your documentation and regulatory needs.


WHY CHOOSE RESOLVEMASS LABORATORIES?

  • Expertise in specialty intermediates: High-purity materials designed for advanced synthesis

  • Reliable supply: Consistent quality backed by rigorous testing

  • Responsive support: Technical assistance and documentation tailored to your project

For pricing, lead times, and custom requests, contact our sales team at ResolveMass Laboratories Inc. or submit an inquiry via resolvemass.ca.

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