180-50-7 Usage
Uses
Used in Pharmaceutical Synthesis:
2,8-DIAZASPIRO[5,5]UNDECANE is used as a key intermediate in the synthesis of various pharmaceuticals for its ability to contribute to the development of new drugs with improved efficacy and selectivity.
Used in Agrochemical Production:
In the agrochemical industry, 2,8-DIAZASPIRO[5,5]UNDECANE is utilized as a building block for the creation of novel agrochemicals, potentially enhancing crop protection and yield.
Used in Fine Chemicals Synthesis:
2,8-DIAZASPIRO[5,5]UNDECANE is employed as a crucial component in the synthesis of fine chemicals, contributing to the advancement of specialty chemicals for various applications.
Used as a Chiral Auxiliary in Asymmetric Synthesis:
2,8-DIAZASPIRO[5,5]UNDECANE is used as a chiral auxiliary in asymmetric synthesis to facilitate the production of enantiomerically pure compounds, which are essential in various chemical and pharmaceutical processes.
Used in Coordination Chemistry:
In the field of coordination chemistry, 2,8-DIAZASPIRO[5,5]UNDECANE is applied to design and synthesize coordination compounds, potentially leading to new materials with unique properties.
Used in Catalysis:
2,8-DIAZASPIRO[5,5]UNDECANE is utilized in catalysis as a component of catalysts, potentially improving the efficiency and selectivity of chemical reactions in various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 180-50-7 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 1,8 and 0 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 180-50:
(5*1)+(4*8)+(3*0)+(2*5)+(1*0)=47
47 % 10 = 7
So 180-50-7 is a valid CAS Registry Number.
InChI:InChI=1/C9H18N2/c1-3-9(7-10-5-1)4-2-6-11-8-9/h10-11H,1-8H2
180-50-7Relevant 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.
