77415-72-6 Usage
Uses
Used in Pharmaceutical Industry:
2,7-DIBENZYL-2,7-DIAZA-SPIRO[4.4]NONANE is used as a building block for the synthesis of complex organic molecules and pharmaceutical compounds. Its unique structure and properties make it a valuable component in the development of new drugs and therapeutic agents.
Used in Materials Science:
2,7-DIBENZYL-2,7-DIAZA-SPIRO[4.4]NONANE is used in the development of advanced materials. Its potential applications in this field include the creation of new materials with improved properties, such as enhanced stability, reactivity, or selectivity.
Used in Research Applications:
2,7-DIBENZYL-2,7-DIAZA-SPIRO[4.4]NONANE is used in various research applications, where its unique structure and properties are leveraged to explore new chemical reactions, mechanisms, and processes. 2,7-DIBENZYL-2,7-DIAZA-SPIRO[4.4]NONANE serves as a valuable tool for scientists in understanding and advancing the field of chemistry and related disciplines.
Check Digit Verification of cas no
The CAS Registry Mumber 77415-72-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,7,4,1 and 5 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 77415-72:
(7*7)+(6*7)+(5*4)+(4*1)+(3*5)+(2*7)+(1*2)=146
146 % 10 = 6
So 77415-72-6 is a valid CAS Registry Number.
77415-72-6Relevant academic research and scientific papers
Quinolone Antibacterial Agents Substituted at the 7-Position with Spiroamines. Synthesis and Structure-Activity Relationships
Culbertson, Townley P.,Sanchez, Joseph P.,Gambino, Laura,Sesnie, Josephine A.
, p. 2270 - 2275 (2007/10/02)
A series of fluoroquinolone antibacterials having the 7-position (10-position of pyridobenzoxazines) substituted with 2,7-diazaspirononane (4b), 1,7-diazaspirononane (5a), or 2,8-diazaspiroundecane (6b) was prepared, and their biological activities were compared with piperazine and pyrrolidine substituted analogues.Most exhibited potent Gram-positive and Gram-negative activity, especially when side chain 4b was N-alkylated.
