78344-54-4

Basic information

• Product Name: 2-oxo-5'-phenylindoline-3-spiro-2'-(1',3',4'-thiadiazol-4'-ine)
• Synonyms: 2-oxo-5'-phenylindoline-3-spiro-2'-(1',3',4'-thiadiazol-4'-ine)
• CAS NO: 78344-54-4
• Molecular Weight: 281.338
• Mol File: 78344-54-4.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: 2-oxo-5'-phenylindoline-3-spiro-2'-(1',3',4'-thiadiazol-4'-ine)(CAS DataBase Reference)
• NIST Chemistry Reference: 2-oxo-5'-phenylindoline-3-spiro-2'-(1',3',4'-thiadiazol-4'-ine)(78344-54-4)
• EPA Substance Registry System: 2-oxo-5'-phenylindoline-3-spiro-2'-(1',3',4'-thiadiazol-4'-ine)(78344-54-4)

Safety Data

• Hazardous Substances Data: 78344-54-4(Hazardous Substances Data)

Upstream product

• 121-68-6 dithiobenzoic acid 
• 62-53-3 aniline 
• 108-86-1 bromobenzene 
• 942-91-6 Carboxymethyl dithiobenzoate 
• 100-52-7 benzaldehyde 
• 15563-40-3 N-thiobenzoylpiperidine 
• 20605-40-7 thiobenzoylhydrazine 
• 91-56-5 indole-2,3-dione 

Relevant articles and documents

Spiro indolone compound as well as, preparation, method and pharmaceutical composition and application thereof

Spiro indolone compounds, a preparing method, a medicine composition and uses of the compounds are disclosed. In particular, the invention provide spiro indolone compounds shown as a formula I or II, a preparing method of the spiro indolone compounds and

Thiadiazole compounds and methods of use thereof

The present invention relates to Thiadiazole Compounds; compositions comprising an effective dose of a Thiadiazole Compound; and methods treating or preventing a metalloproteinase-related disorder, such as, an arthritic disorder, osteoarthritis, cancer, r

SEMICARBAZONES AND THIOSEMICARBAZONES OF THE HETEROCYCLIC SERIES. XLIV. CYCLIZATION OF ISATIN AND 1-ACETYLISATIN 3-THIOBENZOYLHYDRAZONES

Isatin 3-thiobenzoylhydrazone undergoes cyclization with the addition of the sulfur atom to the C3 atom and closure of the thiadiazole ring.In contrast, 3-thioaroylhydrazones of 1-acetylisatin undergo cyclization with participation of C2 and close the thiadiazine ring with the formation of derivatives of the new heterocyclic system thiadiazinoindole.