30536-22-2

Basic information

• Product Name: 4-nitrobenzo[c][1,2,5]thiadiazol-5-aMine
• Synonyms: 4-nitrobenzo[c][1,2,5]thiadiazol-5-aMine
• CAS NO: 30536-22-2
• Molecular Formula: C₆H₄N₄O₂S
• Molecular Weight: 196.18656
• Mol File: 30536-22-2.mol
• Article Data: 4

Chemical Properties

• Appearance: /
• Storage Temp.: 2-8°C
• CAS DataBase Reference: 4-nitrobenzo[c][1,2,5]thiadiazol-5-aMine(CAS DataBase Reference)
• NIST Chemistry Reference: 4-nitrobenzo[c][1,2,5]thiadiazol-5-aMine(30536-22-2)
• EPA Substance Registry System: 4-nitrobenzo[c][1,2,5]thiadiazol-5-aMine(30536-22-2)

Safety Data

• Hazardous Substances Data: 30536-22-2(Hazardous Substances Data)

Upstream product

• 6583-06-8 4-nitro-1,2,3-benzothiadiazole 
• 2274-89-7 5-chloro-4-nito-2,1,3-benzothiadiazole 
• 72023-79-1 5-bromo-4-nitro-benzo[1,2,5]thiadiazole 
• 99-56-9 4-Nitrophenylene-1,2-diamine 
• 16252-88-3 5-nitro-2,1,3-benzothiadiazole 
• 874-37-3 benzo[1,2,5]thiadiazol-5-ylamine 
• 21110-91-8 5-acetamidobenzo-2,1,3-thiadiazole 

Downstream Products

• 1711-66-6 benzo[1,2,5]thiadiazole-4,5-diamine 
• 211-16-5 benzo[1,2-c:3,4-c']bis(1,2,5)thiadiazole 
• 100264-68-4 7,8-diphenyl-[1,2,5]thiadiazolo[3,4-f]quinoxaline 

Relevant articles and documents

Benzothiadiazole compound and preparation method and use thereof

The present invention relates to a benzothiadiazole compound represented by the following formula I, and a preparation method and use thereof, the benzothiadiazole compound has the biological activityof inhibiting protein-tyrosine-phosphatase SHP2, can be used as a tool compound to study the biological functional relevance of the protein-tyrosine-phosphatase SHP2 in a cell signal transduction process, and provides a new means for prevention and treatment of cancer and metabolic and immune diseases.

Synthesis of substituted dipyrido[3,2-a:2′,3′-c]phenazines and a new heterocyclic dipyrido[3,2-f:2′,3′-h]quinoxalino[2,3-b]quinoxaline

Three new α,α′-diimine ligands were synthesized based on condensation of 1,10-phenanthroline-5,6-dione with 1,2-phenylenediamine derivatives using different approaches. All compounds were fully characterized by IR, 1H and 13C NMR, UV-visible, and MS spectroscopies. We report the first example of a dipyrido[3,2-f:2′,3′-h]quinoxalino[2,3-b]quinoxaline, which exhibits a strong absorption at 430 nm and an interesting electrochemical behavior. These new molecules may have biological potential and are of synthetic and technological importance.