105297-10-7 | 4-(4-aminophenyl)thiomorpholine-1,1-dione

Packsize	Purity	Availability	Price	Discounted Price
1g	>98.0%(GC)(T)	in stock	$67.00	$47.00
5g	>98.0%(GC)(T)	in stock	$200.00	$140.00
100g	95%	in stock	$3,091.00	$2,164.00

Description

• Catalog Number: AB65766
• Chemical Name: 4-(4-aminophenyl)thiomorpholine-1,1-dione
• CAS Number: 105297-10-7
• Molecular Formula: C10H14N2O2S
• Molecular Weight: 226.2954
• MDL Number: MFCD06797046
• SMILES: Nc1ccc(cc1)N1CCS(=O)(=O)CC1

Computed Properties

• Complexity: 288
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 15
• Hydrogen Bond Acceptor Count: 4
• Hydrogen Bond Donor Count: 1
• Rotatable Bond Count: 1
• XLogP3: 0.5

Upstream Synthesis Route

The compound 4-(4-Aminophenyl)thiomorpholine 1,1-dioxide, also known as $name$, serves as a versatile building block in chemical synthesis. Due to its unique structure, it finds widespread application as a reagent in organic chemistry processes. Its primary role lies in the formation of complex organic molecules through various reactions such as nucleophilic substitution, condensation, and cyclization.1. Nucleophilic substitution: $name$ can participate in nucleophilic substitution reactions, where the amino group acts as a nucleophile attacking electrophilic centers in the substrate molecule. This enables the introduction of the $name$ moiety into the target molecule, leading to the formation of new carbon-nitrogen bonds.2. Condensation reactions: $name$ can undergo condensation reactions with carbonyl compounds, forming imine derivatives. These imines can further react with other functional groups present in the molecule, allowing for the production of more complex structures.3. Cyclization reactions: The thiomorpholine ring in $name$ provides an inherent cyclic structure that can participate in cyclization reactions. By activating specific functional groups within the molecule, $name$ can facilitate the formation of cyclic compounds with diverse applications in medicinal chemistry and material science.4. Metal-catalyzed transformations: $name$ can also serve as a ligand in metal-catalyzed transformations, enhancing the selectivity and efficiency of certain chemical reactions. The presence of the thiomorpholine dioxide moiety can influence the metal coordination environment, leading to unique reactivity patterns.Overall, the versatility of 4-(4-Aminophenyl)thiomorpholine 1,1-dioxide makes it a valuable tool in chemical synthesis, enabling the construction of complex molecules with precise control over stereochemistry and functional group placement.