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5925-55-3

2-Methyl-2-propylbenzodithiolate

Catalog#: AR00EF7B  |   CAS#: 5925-55-3  |   MDL#: MFCD27978410  |   MF: C11H14S2  |   MW: 210.3589

Packsize Purity Price Availability Quantity
50mg 95% $43.00 Global Stock Buy Now Add To Cart
250mg 95% $129.00 Global Stock Buy Now Add To Cart
1g 95% $398.00 Global Stock Buy Now Add To Cart
5g 95% $1,575.00 Global Stock Buy Now Add To Cart
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Catalog Number AR00EF7B
Chemical Name 2-Methyl-2-propylbenzodithiolate
CAS Number 5925-55-3
Molecular Formula C11H14S2
Molecular Weight 210.3589
MDL Number MFCD27978410
SMILES S=C(c1ccccc1)SC(C)(C)C

Tert-Butyl benzodithioate, also known as TBDT, is a versatile chemical reagent commonly used in organic synthesis. This compound plays a crucial role in the formation of carbon-sulfur bonds, making it a valuable tool in the preparation of various sulfur-containing compounds. In organic chemistry, the application of TBDT is particularly significant in the synthesis of thioethers, thioesters, and other sulfur-containing molecules.One of the primary uses of tert-Butyl benzodithioate is in the Mitsunobu reaction, a powerful method for the inversion of alcohol configurations. By employing TBDT, chemists can facilitate the efficient conversion of primary and secondary alcohols into a wide range of desired products, including esters, ethers, and sulfides. Additionally, TBDT can serve as a sulfur transfer reagent, enabling the introduction of sulfur functional groups into organic molecules with high selectivity and efficiency.Moreover, tert-Butyl benzodithioate is an essential building block in the synthesis of pharmaceuticals, agrochemicals, and materials with sulfur-containing moieties. Its reactivity and compatibility with a variety of functional groups make it a preferred reagent for chemists seeking to introduce sulfur atoms into target molecules while maintaining overall synthetic efficiency.Overall, tert-Butyl benzodithioate is a valuable reagent in chemical synthesis, offering chemists a powerful tool for the construction of complex organic molecules containing sulfur functionalities. Its diverse applications and ability to facilitate challenging transformations make it a cornerstone in the toolkit of synthetic chemists seeking to access a wide array of sulfur-containing compounds.
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