885519-20-0

Basic information

• Product Name: 6-Amino-3-iodo-1H-indazol...
• Synonyms: 6-Amino-3-iodo-1H-indazol...;3-iodo-1H-indazol-6-aMine;3-Iodo-1H-indazol-6-ylaMine
• CAS NO: 885519-20-0
• Molecular Formula: C7H6IN3
• Molecular Weight: 259
• Mol File: 885519-20-0.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 452.2±25.0 °C(Predicted)
• Appearance: /
• Density: 2.168±0.06 g/cm3(Predicted)
• PKA: 13.65±0.40(Predicted)
• CAS DataBase Reference: 6-Amino-3-iodo-1H-indazol...(CAS DataBase Reference)
• NIST Chemistry Reference: 6-Amino-3-iodo-1H-indazol...(885519-20-0)
• EPA Substance Registry System: 6-Amino-3-iodo-1H-indazol...(885519-20-0)

Safety Data

• Hazardous Substances Data: 885519-20-0(Hazardous Substances Data)

Usage

General Description

6-Amino-3-iodo-1H-indazole is a chemical compound with a molecular formula of C7H6IN3. This organic compound belongs to the class of organic compounds known as indazoles, which are aromatic heterocyclic compounds containing a pyrazole ring fused to a benzene ring. It's an important chemical intermediate used in the manufacturing of various pharmaceutical and medicinal products, given its properties. While specific information about its toxicity, safety, or potential side effects is not readily available, as with all chemicals, it should be handled with caution to prevent any potential harm or unwanted reactions.

Upstream product

• 70315-70-7 3-iodo-6-nitro-1H-indazole 
• 7597-18-4 6-nitroindazole 

Relevant articles and documents

N-indazole substituted thiourea derivatives and preparation method and application thereof

The invention discloses N-indazole substituted thiourea derivatives and a preparation method and application thereof and belongs to the technical field of chemical medicine.The thiourea derivatives are a series of compounds simultaneously containing the 1H-indazole ring structure and the asymmetrical thiourea structure, and the compounds are not reported in the literature.The bioactivity test result analysis of the thiourea derivatives show that the compounds are good in antioxidant activity, the average scavenging rate is above 80%, the scavenging rate of the compound 12b, the compound 12c, and the compound 12d and the compound 12h is higher than 90%, the scavenging activity IC50 of the compound 12h on DPPH is 0.14mg/mL; part of the target compounds has certain inhibition activity on herpes viruses, vaccinia viruses, reoviruses, Coxsackie viruses, Feline coronary herpes viruses, HIV viruses and the like, and the compound 12c and the compound 12n are high in antivirus activity; the synthesized compounds hopefully have new bioactivity which is not expounded, and a certain material basis is provided for the development of new medicine.