C[C@H](O)[C@H](C)[C@@H]1O[C@H]1C[C@H]1CO[C@@H](C\C(C)=C\C2=NC=C(O2)C2=CC=C(S2)[N+]([O-])=O)[C@H](O)[C@@H]1O

InChIKey=AUTPSEXQJQWINW-AQUDXKBXSA-N

C23H30N2O8S

494.56

Organic compounds

Organoheterocyclic compounds

Thiophenes

Nitrothiophenes

Not available

2-nitrothiophenes

Nitroaromatic compounds 2,5-disubstituted oxazoles 2,5-disubstituted thiophenes Oxanes Monosaccharides Heteroaromatic compounds Secondary alcohols 1,2-diols Propargyl-type 1,3-dipolar organic compounds Oxacyclic compounds Azacyclic compounds Dialkyl ethers Epoxides Organic oxoazanium compounds Organic zwitterions Hydrocarbon derivatives Organic salts Organonitrogen compounds Organic oxides

Aromatic heteromonocyclic compounds

2-nitrothiophene - Nitroaromatic compound - 2,5-disubstituted 1,3-oxazole - 2,5-disubstituted thiophene - Monosaccharide - Oxane - Heteroaromatic compound - Azole - Oxazole - 1,2-diol - Organic nitro compound - C-nitro compound - Secondary alcohol - Oxacycle - Dialkyl ether - Oxirane - Ether - Azacycle - Organic oxoazanium - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Allyl-type 1,3-dipolar organic compound - Organic salt - Hydrocarbon derivative - Organonitrogen compound - Organooxygen compound - Organic nitrogen compound - Alcohol - Organic oxygen compound - Organic zwitterion - Organic oxide - Aromatic heteromonocyclic compound

This compound belongs to the class of organic compounds known as 2-nitrothiophenes. These are aromatic heterocyclic compound containing a nitro group attached to a thiophene ring a the 2-position.

Not available