128244-02-0 Usage
General Description
The chemical "2,8-Diazaspiro[5.5]undecane-1,7-dione, 2,8-bis(phenylmethyl)-" is a compound with the molecular formula C27H28N2O2. It is a spiro compound, meaning it contains a fused ring system in which two non-adjacent carbon atoms are common to two rings. This specific chemical is characterized by the presence of two phenylmethyl groups at the 2 and 8 positions of the molecule. The compound is used in the field of organic chemistry as a building block for the synthesis of various types of complex organic molecules. Additionally, it may have potential applications in pharmaceutical research and drug discovery due to its unique structure and 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
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.
