1263296-82-7 Usage
Uses
Used in Pharmaceutical Research:
2-Benzhydryl-2-azaspiro[3.3]heptan-5-amine is utilized as a research compound for exploring its pharmacological properties and potential applications in the development of new medications. Its unique structure allows it to be studied for interactions with biological targets, which could lead to the discovery of novel therapeutic agents.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, 2-benzhydryl-2-azaspiro[3.3]heptan-5-amine serves as a key intermediate or building block in the synthesis of more complex molecules with specific biological activities. Its presence in these molecules can influence their pharmacokinetics, pharmacodynamics, and overall efficacy.
Used in Drug Design and Development:
2-Benzhydryl-2-azaspiro[3.3]heptan-5-amine is employed as a component in drug design, where its incorporation into new chemical entities can enhance their binding affinity to target proteins or receptors. This can result in improved potency, selectivity, and therapeutic index for the treatment of various diseases.
Note: Since the provided materials do not specify particular applications or industries for 2-benzhydryl-2-azaspiro[3.3]heptan-5-amine, the uses listed are general and based on the potential of such a compound in the field of medicinal chemistry and pharmaceutical research.
Check Digit Verification of cas no
The CAS Registry Mumber 1263296-82-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,6,3,2,9 and 6 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1263296-82:
(9*1)+(8*2)+(7*6)+(6*3)+(5*2)+(4*9)+(3*6)+(2*8)+(1*2)=167
167 % 10 = 7
So 1263296-82-7 is a valid CAS Registry Number.
1263296-82-7Relevant academic research and scientific papers
Synthesis of novel angular spirocyclic azetidines
Guerot, Carine,Tchitchanov, Boris H.,Knust, Henner,Carreira, Erick M.
, p. 780 - 783 (2011/05/05)
The syntheses of a variety of novel angular azaspiro[3.3]heptanes are reported. gem-Difluoro and gem-dimethyl variants of the angular 1,6-diazaspiro[3.3]heptane module were prepared in high yields using efficient sequences. Additionally, a practical one-p
