18709-44-9 Usage
Uses
Used in Organic Synthesis:
3-(Phenylmethyl)-2H-azirine is utilized as a reactive intermediate for the synthesis of various organic compounds. Its high reactivity allows it to participate in a multitude of chemical reactions, facilitating the creation of complex organic molecules.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, 3-(Phenylmethyl)-2H-azirine is employed as a building block for the development of pharmaceutical agents. Its unique structure and reactivity can be leveraged to design and synthesize novel drug candidates with potential therapeutic applications.
Used in Chemical Research:
3-(Phenylmethyl)-2H-azirine serves as a subject of study in chemical research, where its reactivity and chemical behavior are explored to understand and expand the knowledge of azirine chemistry and its implications in various chemical processes.
Used in Specialty Chemicals Production:
3-(Phenylmethyl)-2H-azirine is used as a key component in the production of specialty chemicals that require the unique properties of aziridines, such as specific types of polymers, agrochemicals, and other high-value chemical products.
Check Digit Verification of cas no
The CAS Registry Mumber 18709-44-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,7,0 and 9 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 18709-44:
(7*1)+(6*8)+(5*7)+(4*0)+(3*9)+(2*4)+(1*4)=129
129 % 10 = 9
So 18709-44-9 is a valid CAS Registry Number.
18709-44-9Relevant academic research and scientific papers
Exploiting the chemistry of strained rings: Synthesis of indoles via domino reaction of aryl iodides with 2 H-azirines
Candito, David A.,Lautens, Mark
supporting information; experimental part, p. 3312 - 3315 (2010/10/19)
(Equation Presented). The highly strained 2H-azirine ring system has been the source of considerable theoretical and synthetic work. The reaction of these strained heterocycles with transition metals has been documented to give rise to ring opening and subsequent formation of varied heterocycles. An interesting domino reaction is described wherein the strained bicyclic alkene, norbornene, mediates the reaction of 2H-azirines with aryl iodides under palladium catalysis to provide indole or polycyclic dihydroimidazole heterocycles.
