CCOC1=CC(C=C2C(=O)NC(=S)N(C2=O)C2=CC=CC(=C2)C(O)=O)=CC(CC=C)=C1OCC1=CC=C(C=C1)[N+]([O-])=O

InChIKey=SFMUGCQVOSBUMQ-UHFFFAOYSA-N

C30H25N3O8S

587.6

Organic compounds

Benzenoids

Benzene and substituted derivatives

Benzoic acids and derivatives

Not available

Acylaminobenzoic acid and derivatives

N-phenylthioureas Thiobarbituric acid derivatives Benzoic acids Nitrobenzenes Phenoxy compounds Phenol ethers Benzoyl derivatives Nitroaromatic compounds Alkyl aryl ethers Diazinanes Thioureas Propargyl-type 1,3-dipolar organic compounds Azacyclic compounds Carboxylic acids Organic oxoazanium compounds Organonitrogen compounds Carbonyl compounds Organic salts Hydrocarbon derivatives Organic zwitterions Organic oxides

Aromatic heteromonocyclic compounds

Acylaminobenzoic acid or derivatives - N-phenylthiourea - Benzoic acid - Nitrobenzene - Thiobarbiturate - Phenoxy compound - Nitroaromatic compound - Benzoyl - Phenol ether - Alkyl aryl ether - 1,3-diazinane - C-nitro compound - Organic nitro compound - Thiourea - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Allyl-type 1,3-dipolar organic compound - Organoheterocyclic compound - Carboxylic acid derivative - Carboxylic acid - Ether - Organic oxoazanium - Azacycle - Organic zwitterion - Organic nitrogen compound - Organonitrogen compound - Hydrocarbon derivative - Organooxygen compound - Organosulfur compound - Carbonyl group - Organic oxide - Organic salt - Organic oxygen compound - Aromatic heteromonocyclic compound

This compound belongs to the class of organic compounds known as acylaminobenzoic acid and derivatives. These are derivatives of amino benzoic acid derivatives where the amine group is N-acylated.

Not available