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(3R,4S,5R,6R)-3,4,5-tris(triMethylsilyloxy)-6-((triMethylsilyloxy)Methyl)tetrahydro-2H-pyran-2-one CAS: 32384-65-9

Short Description:

Catalog Number: XD93606
Cas: 32384-65-9
Molecular Formula: C4H8O2
Molecular Weight: 88.11
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Product Tags

Catalog Number XD93606
Product Name (3R,4S,5R,6R)-3,4,5-tris(triMethylsilyloxy)-6-((triMethylsilyloxy)Methyl)tetrahydro-2H-pyran-2-one
CAS 32384-65-9
Molecular Formula C4H8O2
Molecular Weight 88.11
Storage Details Ambient

 

Product Specification

Appearance White powder
Assay 99% min

 

(3R,4S,5R,6R)-3,4,5-tris(triMethylsilyloxy)-6-((triMethylsilyloxy)Methyl)tetrahydro-2H-pyran-2-one, also known as TBDMS-protected tetrahydro-2H-pyran-2-one, is a compound commonly used in organic synthesis and as a protecting group in the field of chemistry.One important application of TBDMS-protected tetrahydro-2H-pyran-2-one is its use as a building block in the synthesis of complex organic molecules. The compound possesses multiple reactive sites that can undergo various functional group transformations. The TBDMS (tert-butyldimethylsilyl) protecting group present in the molecule provides stability and allows for selective modification of specific functional groups. This versatility makes TBDMS-protected tetrahydro-2H-pyran-2-one a valuable intermediate in the synthesis of natural products, pharmaceuticals, and other fine chemicals.Another significant use of TBDMS-protected tetrahydro-2H-pyran-2-one is its role as a protecting group for alcohols and amines in organic synthesis. The TBDMS group can be selectively added to hydroxyl or amino groups, effectively masking them during various reaction steps. This protection prevents unwanted side-reactions and ensures the desired transformations occur at the desired sites. Once the desired reactions are complete, the TBDMS group can be easily removed, exposing the original hydroxyl or amino group without affecting other functionalities in the molecule.TBDMS-protected tetrahydro-2H-pyran-2-one also finds application as a protective agent for carbohydrates. It allows for the selective protection of hydroxyl groups in sugar molecules during glycosylation reactions, enabling the synthesis of complex glycans and glycosides. This protection strategy is particularly important in carbohydrate chemistry, where multiple hydroxyl groups are present and specific regioselectivity is required.Furthermore, TBDMS-protected tetrahydro-2H-pyran-2-one is utilized in the preparation of functionalized polymers. The compound can be incorporated into polymer structures, providing reactive sites for further modifications and cross-linking reactions. This enables the creation of polymer materials with tailored properties and functionalities, such as improved stability, biocompatibility, and controlled drug release.In conclusion, (3R,4S,5R,6R)-3,4,5-tris(triMethylsilyloxy)-6-((triMethylsilyloxy)Methyl)tetrahydro-2H-pyran-2-one, or TBDMS-protected tetrahydro-2H-pyran-2-one, is a versatile compound with various applications in organic synthesis, especially as a building block and protecting group. Its ability to selectively protect functional groups and facilitate complex molecular transformations makes it a valuable tool in the field of chemistry. Continued research and exploration of its applications may uncover further uses and contribute to advancements in synthetic chemistry and material science.


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    (3R,4S,5R,6R)-3,4,5-tris(triMethylsilyloxy)-6-((triMethylsilyloxy)Methyl)tetrahydro-2H-pyran-2-one CAS: 32384-65-9