AB43669
Packsize | Purity | Availability | Price | Discounted Price | Quantity | |
---|---|---|---|---|---|---|
5g | tech | in stock | $15.00 | $10.00 | - + | |
25g | tech | in stock | $16.00 | $11.00 | - + | |
50g | tech | in stock | $30.00 | $21.00 | - + | |
100g | tech | in stock | $46.00 | $32.00 | - + | |
500g | tech | in stock | $210.00 | $147.00 | - + |
*All products are for research use only and not intended for human or animal use.
*All prices are in USD.
Catalog Number: | AB43669 |
Chemical Name: | 1,4-Dithiane-2,5-diol |
CAS Number: | 40018-26-6 |
Molecular Formula: | C4H8O2S2 |
Molecular Weight: | 152.2351 |
MDL Number: | MFCD00006659 |
SMILES: | OC1SCC(SC1)O |
1,4-Dithiane-2,5-diol, also known as DTD, is a versatile compound widely used in chemical synthesis. Its unique structure containing dithiane and diol functionalities imparts valuable properties that make it a valuable building block for organic chemists. In particular, 1,4-Dithiane-2,5-diol is commonly employed as a protecting group for aldehydes and ketones in organic synthesis. By selectively masking the carbonyl group with a DTD moiety, chemists can manipulate the reactivity of the carbonyl functionality, allowing for the selective modification of other functional groups in a molecule. This protection strategy is crucial in complex organic synthesis to prevent unwanted side reactions or unwanted interactions with reagents. Moreover, 1,4-Dithiane-2,5-diol can also serve as a valuable precursor for the synthesis of various heterocyclic compounds, such as dithiane derivatives and cyclic ethers. Its ability to form stable complexes with transition metals further expands its utility in metal-catalyzed reactions, enabling the efficient formation of new carbon-carbon and carbon-heteroatom bonds. Overall, 1,4-Dithiane-2,5-diol plays a pivotal role in modern organic synthesis by offering chemists a robust tool for protecting reactive functional groups and enabling the synthesis of diverse molecular architectures.