128244-02-0 Usage
Uses
Used in Organic Chemistry:
2,8-Diazaspiro[5.5]undecane-1,7-dione, 2,8-bis(phenylmethyl)is used as a building block for the synthesis of complex organic molecules. Its spiro structure and phenylmethyl groups provide versatility in the creation of diverse chemical entities.
Used in Pharmaceutical Research and Drug Discovery:
Due to its unique structural features, 2,8-Diazaspiro[5.5]undecane-1,7-dione, 2,8-bis(phenylmethyl)may be utilized as a starting material or intermediate in the development of new pharmaceutical compounds. Its potential applications in this field could include the design of novel drugs with specific therapeutic targets or properties.
Check Digit Verification of cas no
The CAS Registry Mumber 128244-02-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,8,2,4 and 4 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 128244-02:
(8*1)+(7*2)+(6*8)+(5*2)+(4*4)+(3*4)+(2*0)+(1*2)=110
110 % 10 = 0
So 128244-02-0 is a valid CAS Registry Number.
InChI:InChI=1/C23H26N2O2/c26-21-23(13-7-15-24(21)17-19-9-3-1-4-10-19)14-8-16-25(22(23)27)18-20-11-5-2-6-12-20/h1-6,9-12H,7-8,13-18H2
128244-02-0Relevant articles and documents
Dispiromacrocycles: A class of diamide and diimide ionophores
Bell,Choi,Hiel
, p. 971 - 974 (2007/10/02)
A series of novel ionophores was synthesized in three steps from acrylonitrile and diethyl malonate or malononitrile via 2,8-diazaspiro[5,5]undecane-1,7-dione (7) or 2,8-diazaspiro[5,5]undecane-1,3,7,9-tetrone (8). Spirodiamide macrocycle 14 imparts selec
Cyclic compounds for complexing with cations
-
, (2008/06/13)
Cyclic molecules having oriented groups are capable of forming stable complexes with cations.
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.
