7764-29-6 | N,N'-Thio-bis(phthalimide)

Packsize	Purity	Availability	Price	Discounted Price
1g	97%	in stock	$74.00	$52.00
5g	97%	in stock	$222.00	$156.00

Description

• Catalog Number: AB48200
• Chemical Name: N,N'-Thio-bis(phthalimide)
• CAS Number: 7764-29-6
• Molecular Formula: C16H8N2O4S
• Molecular Weight: 324.3107
• MDL Number: MFCD00014581
• SMILES: O=C1N(SN2C(=O)c3c(C2=O)cccc3)C(=O)c2c1cccc2

Upstream Synthesis Route

The compound 2,2'-Thiobis[1H-isoindole-1,3(2H)-dione], commonly referred to as $name$, serves as a versatile reagent in chemical synthesis. Its unique structure containing a sulfur atom within an isoindole ring provides it with special chemical reactivity that is valuable in various synthetic applications.In organic synthesis, $name$ is often employed as a key building block in the construction of complex molecules. Its sulfur-containing ring system can participate in a variety of reactions, including nucleophilic substitution and oxidative coupling reactions, enabling the formation of new bonds and the creation of structurally diverse compounds.One notable application of $name$ is in the synthesis of heterocyclic compounds with pharmacological importance. By incorporating $name$ into a synthetic pathway, chemists can access a wide range of bioactive molecules with potential medicinal properties. Additionally, the presence of the isoindole moiety in $name$ can impart interesting electronic and steric effects to the target molecules, further expanding the scope of synthetic possibilities.Furthermore, the sulfur atom in $name$ offers the opportunity for further functionalization through sulfonation or oxidation reactions, allowing for the modification of its chemical properties and the customization of its reactivity in a given synthesis.Overall, the use of 2,2'-Thiobis[1H-isoindole-1,3(2H)-dione] in chemical synthesis highlights its significance as a valuable tool for the creation of novel organic compounds with diverse applications in fields such as pharmaceuticals, materials science, and agrochemicals.