CC(C)(C)CCN1C(=O)\C(C(O)=C1C(C)(C)C)=C1/Nc2ccc(NS(C)(=O)=O)cc2[P@](=O)(N1)OCCCO[Si](C)(C)C(C)(C)C

InChIKey=PCSOUGZYWCYIDM-BWYLKJKOSA-N

C31H53N4O7PSSi

684.9

Organic compounds

Benzenoids

Benzene and substituted derivatives

Sulfanilides

Not available

Sulfanilides

Organic sulfonamides Organosulfonamides Phosphonic acid esters Phosphonic amide esters Pyrrolines Aminosulfonyl compounds Tertiary carboxylic acid amides Trialkylheterosilanes Vinylogous amides Lactams Ketene acetals Silyl ethers Azacyclic compounds Phosphacyclic compounds Organic metalloid salts Carbonyl compounds Amines Organic oxides Hydrocarbon derivatives

Aromatic heteropolycyclic compounds

Sulfanilide - Organosulfonic acid amide - Phosphonic amide ester - Organic sulfonic acid amide - Phosphonic acid ester - Sulfonyl - Tertiary carboxylic acid amide - Aminosulfonyl compound - Organosulfonic acid or derivatives - Organophosphonic acid derivative - Pyrroline - Organic sulfonic acid or derivatives - Trialkylheterosilane - Vinylogous amide - Carboxamide group - Lactam - Ketene acetal or derivatives - Silyl ether - Carboxylic acid derivative - Organoheterosilane - Phosphacycle - Azacycle - Organic metalloid salt - Organoheterocyclic compound - Organosulfur compound - Organooxygen compound - Organonitrogen compound - Organic oxide - Organic metalloid moeity - Hydrocarbon derivative - Carbonyl group - Organic nitrogen compound - Amine - Organic oxygen compound - Organosilicon compound - Aromatic heteropolycyclic compound

This compound belongs to the class of organic compounds known as sulfanilides. These are organic aromatic compounds containing a sulfanilide moiety, with the general structure RS(=O)(=O)NC1=CC=CC=C1.

Not available