118837-66-4 | N-Isopropyl 3-aminobenzenesulfonamide

Packsize	Purity	Availability	Price	Discounted Price
1g	98%	in stock	$105.00	$74.00
5g	98%	in stock	$318.00	$223.00
25g	98%	in stock	$1,131.00	$792.00

Description

• Catalog Number: AE10408
• Chemical Name: N-Isopropyl 3-aminobenzenesulfonamide
• CAS Number: 118837-66-4
• Molecular Formula: C9H14N2O2S
• Molecular Weight: 214.2847
• MDL Number: MFCD09027278
• SMILES: CC(NS(=O)(=O)c1cccc(c1)N)C

Computed Properties

• Complexity: 269
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 14
• Hydrogen Bond Acceptor Count: 4
• Hydrogen Bond Donor Count: 2
• Rotatable Bond Count: 3
• XLogP3: 0.8

Upstream Synthesis Route

3-Amino-N-isopropylbenzenesulfonamide, often referred to as $name$, is a versatile compound widely used in chemical synthesis processes. This compound is specifically valued for its ability to serve as a key building block in the creation of various pharmaceuticals and agrochemicals through the formation of new chemical bonds. Its unique structure allows for the modification of functional groups, enabling the synthesis of diverse molecules with enhanced properties.In chemical synthesis, $name$ acts as a crucial intermediate in the preparation of sulfonamide-based compounds, which are commonly employed as antimicrobial agents, inhibitors, and pharmaceutical ingredients. By incorporating $name$ into a synthetic pathway, chemists can efficiently access a range of biologically active molecules with the desired structural features. The presence of the amino and sulfonamide functionalities in $name$ enables selective reactions with other reagents, facilitating the creation of complex organic compounds.Moreover, the utilization of 3-Amino-N-isopropylbenzenesulfonamide in chemical synthesis extends beyond pharmaceuticals to include the development of novel materials and specialty chemicals. Its versatile nature and reactivity make it a valuable tool for constructing intricate molecular architectures and exploring new avenues for molecular design in the field of organic chemistry. By leveraging the synthetic capabilities of $name$, researchers can advance their studies in drug discovery, materials science, and other interdisciplinary areas, paving the way for innovative solutions and applications in various industries.