19230-34-3 Usage
Uses
Used in Coordination Chemistry:
3,4-BIS-DIMETHYLAMINO-CYCLOBUT-3-ENE-1,2-DIONE is used as a ligand for forming complexes with metal ions. Its ability to coordinate with metal ions makes it a valuable component in the development of new materials with specific properties.
Used in Organic Synthesis:
3,4-BIS-DIMETHYLAMINO-CYCLOBUT-3-ENE-1,2-DIONE serves as a building block in the synthesis of various organic compounds and pharmaceuticals. Its unique structure allows for the creation of a wide range of molecules with potential applications in different industries.
Used in Materials Science:
3,4-BIS-DIMETHYLAMINO-CYCLOBUT-3-ENE-1,2-DIONE has potential applications in materials science due to its unique molecular structure. It can be used to develop new materials with specific properties, such as improved conductivity or stability.
Used in Electrochemistry:
3,4-BIS-DIMETHYLAMINO-CYCLOBUT-3-ENE-1,2-DIONE also has potential applications in electrochemistry. Its properties can be harnessed to develop new electrochemical devices or improve the performance of existing ones.
Check Digit Verification of cas no
The CAS Registry Mumber 19230-34-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,2,3 and 0 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 19230-34:
(7*1)+(6*9)+(5*2)+(4*3)+(3*0)+(2*3)+(1*4)=93
93 % 10 = 3
So 19230-34-3 is a valid CAS Registry Number.
InChI:InChI=1/C8H12N2O2/c1-9(2)5-6(10(3)4)8(12)7(5)11/h1-4H3
19230-34-3Relevant academic research and scientific papers
Fu, Nanyan,Allen, Annette D.,Kobayashi, Shinjiro,Tidwell, Thomas T.,Vukovic, Sinisa,Arumugam, Selvananthan,Popik, Vladimir V.,Mishima, Masaaki
, p. 1951 - 1956 (2007)
Hitherto unknown diamino-substituted bisketenes with both free (14) and tethered (16) amino substituents have been generated by using laser flash photolysis for ring opening of the corresponding cyclobutenediones. The time-resolved kinetics of ring closur
A new mode of cyclobutenedione ring opening for the synthesis of 2-oxobut-3-enamides and tetrasubstituted furans
Bennett, Ryan M.,Sun, Wei,Wilson, Dharyl C.,Light, Mark E.,Harrowven, David C.
supporting information, p. 5694 - 5697 (2021/06/16)
A dichotomy between the additions of organolithiums and lithium amides to cyclobutenediones is described wherein the former give carbonyl addition products while the latter induce ring opening by enone cleavagevia O- toC-lithium transfer. This distinct mode of ring scission gives access to 2-oxobut-3-enamides and tetrasubstituted furans.
