Interesting facts
              Interesting Facts About 5-Nitro-1H-Indazole
5-Nitro-1H-indazole is a fascinating compound that belongs to the indazole class, which is characterized by its unique structure consisting of a five-membered ring containing nitrogen atoms. Here are some compelling insights into this intriguing compound:
- Chemical Structure: The indazole ring structure contributes to the compound's chemical reactivity and biological activity, making it a subject of interest for researchers.
- Biological Significance: It is often studied for its potential applications in pharmacology, especially in developing new drugs due to its ability to interact with biological systems.
- Chemical Reactivity: The nitro group (-NO2) present in 5-nitro-1H-indazole enhances its electrophilic nature, making it a useful intermediate in organic synthesis.
- Research Applications: This compound has been explored in various studies related to cancer treatment and as a scaffold for creating novel anti-tumor agents.
- Literature: Numerous research papers highlight its synthesis methods, reactions, and applications, indicating its growing importance in the field of medicinal chemistry.
5-Nitro-1H-indazole exemplifies how compounds derived from indazole can serve as a foundation for the synthesis of more complex molecules with significant biological activity. Its characteristic features not only make it an interesting subject of study in academic circles but also a potential player in the pharmaceutical industry. As always, the exploration of such compounds pushes the boundaries of what we know about chemistry and its applications!
Synonyms
          5-Nitroindazole
          5-Nitro-1H-indazole
          1H-INDAZOLE, 5-NITRO-
          CCRIS 4134
          NSC 5032
          EINECS 226-451-5
          UNII-235Y7P37ZD
          BRN 0007936
          DTXSID5049316
          5-NITRO-1H-BENZOPYRAZOLE
          235Y7P37ZD
          NSC-5032
          NITROINDAZOLE, 5-
          INDAZOLE, 5-NITRO-
          DTXCID4029272
          5-23-06-00180 (Beilstein Handbook Reference)
          5Nitro1Hindazole
          Nitroindazole, 5
          1HIndazole, 5nitro
          Nitro1Hindazole, 5
          226-451-5
          inchi=1/c7h5n3o2/c11-10(12)6-1-2-7-5(3-6)4-8-9-7/h1-4h,(h,8,9
          wsguraytcuvdql-uhfffaoysa-n
          5401-94-5
          5-nitro-1H-indazol
          5-nitro-indazole
          MFCD00005693
          CHEMBL165372
          5NI
          5-nitro-2H-indazole
          5-Nitroindazol
          5-nitro indazole
          5-nitro-IH-indazole
          4lm0
          5-Nitroindazole, >=99%
          65750-01-8
          MLS000728712
          SCHEMBL148826
          SCHEMBL17594510
          NSC5032
          HMS2699L04
          HMS3604H19
          BCP23472
          CS-B1273
          Tox21_202925
          BDBM50304144
          STK764725
          AKOS000120077
          AKOS015966034
          AKOS024268503
          AC-2732
          DB04534
          FN36705
          PB25890
          NCGC00245898-01
          NCGC00260471-01
          AS-11700
          PD059222
          SMR000306991
          SY002722
          CAS-5401-94-5
          DB-014603
          DB-207167
          N0398
          NS00020000
          EN300-18228
          A829911
          AQ-776/40649175
          Q27253724
          Z57471016
          F0001-1417
              
Solubility of 5-nitro-1H-indazole
The solubility of 5-nitro-1H-indazole can be influenced by several factors, making it an intriguing compound to study in terms of its interaction with various solvents. Here are some key points regarding its solubility:
In conclusion, while 5-nitro-1H-indazole shows limited solubility in water, it tends to dissolve more readily in organic solvents, making it essential for researchers to consider solvent choice and conditions when working with this compound. Understanding its solubility profile is crucial for applications in synthesis and formulation.