CC1=CC=C(SC2=C(C=C(\C=C3/C(=O)N(C(=S)N(C3=O)C3=CC(C)=C(C)C=C3)C3=CC=CC=C3)C=C2)[N+]([O-])=O)C=C1

InChIKey=CHIGATIMTHYMHS-OVVQPSECSA-N

C32H25N3O4S2

579.69

Organic compounds

Organosulfur compounds

Thioethers

Aryl thioethers

Not available

Diarylthioethers

N-phenylthioureas Nitrobenzenes Thiobarbituric acid derivatives Thiophenol ethers o-Xylenes Nitroaromatic compounds Toluenes Diazinanes Thioureas Sulfenyl compounds Propargyl-type 1,3-dipolar organic compounds Carboxylic acids and derivatives Organic oxoazanium compounds Azacyclic compounds Carbonyl compounds Hydrocarbon derivatives Organic oxides Organic salts Organonitrogen compounds Organic cations

Aromatic heteromonocyclic compounds

Diarylthioether - N-phenylthiourea - Nitrobenzene - Thiobarbiturate - Nitroaromatic compound - O-xylene - Xylene - Thiophenol ether - Toluene - Monocyclic benzene moiety - 1,3-diazinane - Benzenoid - C-nitro compound - Organic nitro compound - Thiourea - Carboxylic acid derivative - Azacycle - Organic oxoazanium - Organoheterocyclic compound - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Sulfenyl compound - Allyl-type 1,3-dipolar organic compound - Organonitrogen compound - Carbonyl group - Organooxygen compound - Organic salt - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organic nitrogen compound - Organic cation - Aromatic heteromonocyclic compound

This compound belongs to the class of organic compounds known as diarylthioethers. These are organosulfur compounds containing a thioether group that is substituted by two aryl groups.

Not available