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CAS 16495-03-7

(S)-4-Benzyloxymethyl-2,2-dimethyl-1,3-dioxolane TCI B2137

(S)-4-Benzyloxymethyl-2,2-dimethyl-1,3-dioxolane TCI B2137

Chemical Identity

CAS No.
16495-03-7
PubChem
CID 10878747·SID 87565005
Formula
C13H18O3
Molecular weight
222.28 g/mol
Purity
>98.0%(GC)
Full identifiers (IUPAC, SMILES, InChIKey)
IUPAC
(4S)-2,2-dimethyl-4-(phenylmethoxymethyl)-1,3-dioxolane
SMILES
CC1(OC[C@@H](O1)COCC2=CC=CC=C2)C
InChIKey
DBFDSKSLTCMIPB-LBPRGKRZSA-N
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TCI B2137 16495-03-7 (S)-4-Benzyloxymethyl-2,2-dimethyl-1,3-dioxolane is a chiral building block widely used in asymmetric synthesis to construct complex molecular structures. This compound plays a crucial role in organic chemistry laboratories, where it serves as a key reagent for creating chiral molecules with specific stereochemistry. Its unique structure combines a 1,3-dioxolane ring with a benzyloxymethyl group, offering both stability and reactivity in chemical reactions. This makes it an essential tool for researchers aiming to develop compounds with precise stereochemical configurations.

The compound's chiral nature and structural features make it a preferred choice for synthetic chemists. Its ability to participate in enantioselective reactions allows for the synthesis of optically active compounds, which are vital in pharmaceutical and biochemical research. The presence of the benzyloxymethyl group enhances its reactivity in various functional group transformations, while the 1,3-dioxolane ring provides a stable platform for further modifications. These properties contribute to its reliability and effectiveness in complex synthetic pathways.

In Indonesian laboratories, this compound is commonly used in organic chemistry research, particularly in projects requiring the synthesis of bioactive compounds. Its role in drug development and the creation of pharmacologically active substances makes it a valuable resource for academic and industrial research. The compound's chiral characteristics are especially important in the development of new therapeutic agents, where stereochemistry can significantly impact biological activity.

TCI brochures (PDF)

  • Asymmetric Synthesis: This compound is ideal for enantioselective reactions due to its chiral structure, enabling the synthesis of optically active compounds with high stereocontrol.
  • Organic Chemistry Research: It is widely used in the development of complex molecules, especially those with biological activity, due to its reactivity and structural versatility.
  • Pharmaceutical Development: Its role in creating pharmacologically active substances makes it a key reagent in drug discovery and synthesis projects.
  • Chiral Compound Synthesis: The compound's chiral center allows for the selective formation of specific enantiomers, which is critical in the production of therapeutics with precise stereochemistry.
  • Bioactive Molecule Production: It is frequently employed in the synthesis of compounds with biological activity, supporting research in medicinal chemistry and pharmacology.

Brand TCI
CAS number 16495-03-7
Molecular formula —
Purity —
Category Chemistry > Asymmetric Synthesis > Chiral Building Blocks
Pack sizes —
Physical form —
Storage Store in a cool, dry place away from light and moisture

This compound should be stored in a cool, dry environment, away from direct light and moisture to maintain its chemical integrity. It is recommended to use airtight containers to prevent exposure to air and potential degradation. Due to its chiral nature, it is important to handle the compound with care to avoid contamination or loss of stereochemical purity. In laboratory settings, it should be stored separately from incompatible substances to ensure safety. Proper labeling and documentation are essential to maintain traceability and prevent mix-ups. Regular monitoring of storage conditions is advised to ensure optimal preservation of the compound's properties.

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