21742-05-2 Usage
Explanation
The compound is composed of 8 carbon atoms, 6 hydrogen atoms, 1 fluorine atom, 3 nitrogen atoms, and 1 oxygen atom.
Explanation
The compound has a 1,2,5-oxadiazole core with an amine group attached to the 3rd position and a 2-fluorophenyl substituent at the 4th position.
Explanation
It contains oxygen, nitrogen, and carbon atoms in its ring structure, making it a heterocyclic compound.
Explanation
The compound is derived from the parent compound 1,2,5-oxadiazole by incorporating an amine group and a fluorophenyl substituent.
Explanation
Due to its unique structure and potential biological activity, the compound may have applications in the development of new drugs or therapies.
Explanation
The specific properties, potential uses, and safety of the compound would need to be determined through additional research and testing.
Explanation
The presence of the amine group and fluorophenyl substituent may contribute to the compound's biological activity, which could be relevant for its use in medicinal chemistry and pharmaceuticals.
Explanation
The stability of the compound under various conditions (e.g., temperature, pH, etc.) is not provided and would need to be determined through further research.
Explanation
The solubility of the compound in different solvents (e.g., water, organic solvents) is not provided and would need to be determined through experimentation.
Explanation
The reactivity of the compound with other chemicals or under specific conditions is not provided and would need to be determined through further research.
Structure
1,2,5-Oxadiazol-3-amine, 4-(2-fluorophenyl)-
Heterocyclic Compound
Yes
Derivative
1,2,5-Oxadiazol-3-amine
Potential Applications
Medicinal chemistry and pharmaceuticals
Further Investigation
Required
Biological Activity
Potential
Chemical Stability
Unknown
Solubility
Unknown
Reactivity
Unknown
Check Digit Verification of cas no
The CAS Registry Mumber 21742-05-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,7,4 and 2 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 21742-05:
(7*2)+(6*1)+(5*7)+(4*4)+(3*2)+(2*0)+(1*5)=82
82 % 10 = 2
So 21742-05-2 is a valid CAS Registry Number.
21742-05-2Relevant academic research and scientific papers
Zhilin, Egor S.,Bystrov, Dmitry M.,Ananyev, Ivan V.,Fershtat, Leonid L.,Makhova, Nina N.
, p. 14284 - 14289 (2019)
A novel one-pot cascade method for the assembly of valuable NO-donor azasydnone scaffold has been developed. The construction strategy involves a diazotization/azo coupling/elimination/double rearrangement cascade sequence of readily available amines. The
N -Oxide-Controlled Chemoselective Reduction of Nitrofuroxans
Fershtat, Leonid L.,Bystrov, Dmitry M.,Zhilin, Egor S.,Makhova, Nina N.
, p. 747 - 756 (2019/01/23)
A facile and chemoselective SnCl 2 -mediated mild reduction of regioisomeric 3- and 4-nitrofuroxans for the synthesis of aminofurazans and aminofuroxans in good yields is developed. Reduction of 4-nitrofuroxans results in the selective formation of 4-aminofuroxans, while analogous reduction of 3-nitrofuroxans affords 3-aminofurazans as a result of simultaneous reduction of the nitro group and exocyclic N-O bond.
One-pot synthesis of 3-amino-4-aryl- and 3-amino-4-hetarylfurazans
Sheremetev
, p. 1057 - 1059 (2007/10/03)
A "one pot" method for the synthesis of 3-amino-4-aryl- and 3-amino-4-hetarylfurazans from β-aryl- and 4-β-hetaryl-β-oxo acid esters was developed.
