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.