Sulfamic acid, specifically the compound with the name "Sulfamic acid, [[2,4,6-tris(1-methylethyl)phenyl]acetyl]-, 4-(3-aminopropoxy)-2,6-bis(1-methylethyl)phenyl ester," is a complex organic molecule characterized by its sulfonamide functional group, which contributes to its acidic properties. This compound features a sulfamic acid moiety linked to a phenyl ester structure, indicating potential applications in various chemical reactions and processes. The presence of multiple isopropyl groups on the phenyl rings suggests enhanced hydrophobic characteristics, which may influence its solubility and reactivity in organic solvents. Additionally, the incorporation of an aminopropoxy group indicates potential for interaction with biological systems, making it of interest in medicinal chemistry. The compound's CAS number, 454203-56-6, allows for precise identification and retrieval of information regarding its properties, safety data, and potential applications. Overall, this sulfamic acid derivative exhibits unique structural features that may confer specific chemical behaviors and applications in various fields, including pharmaceuticals and materials science.

Sulfamic acid, [[2,4,6-tris(1-methylethyl)phenyl]acetyl]-, 4-(3-aminopropoxy)-2,6-bis(1-methylethyl)phenyl ester (9CI)

454203-56-6: Sulfamic acid, specifically the compound with the name "Sulfamic acid, [[2,4,6-tris(1-methylethyl)phenyl]acetyl]-, 4-(3-aminopropoxy)-2,6-bis(1-methylethyl)phenyl ester," is a complex organic molecule characterized by its sulfonamide functional group, which contributes to its acidic properties. This compound features a sulfamic acid moiety linked to a phenyl ester structure, indicating potential applications in various chemical reactions and processes. The presence of multiple isopropyl groups on the phenyl rings suggests enhanced hydrophobic characteristics, which may influence its solubility and reactivity in organic solvents. Additionally, the incorporation of an aminopropoxy group indicates potential for interaction with biological systems, making it of interest in medicinal chemistry. The compound's CAS number, 454203-56-6, allows for precise identification and retrieval of information regarding its properties, safety data, and potential applications. Overall, this sulfamic acid derivative exhibits unique structural features that may confer specific chemical behaviors and applications in various fields, including pharmaceuticals and materials science.

<p>ACAT-IN-4 inhibits ACAT and NF-κB-mediated transcription.</p>

CAS 454203-56-6

Sulfamic acid, [[2,4,6-tris(1-methylethyl)phenyl]acetyl]-, 4-(3-aminopropoxy)-2,6-bis(1-methylethyl)phenyl ester (9CI)

ACAT-IN-4

Ref: TM-T40554