21994-41-2 Usage
Description
1-(4-cyanobutyl)triaza-1,2-dien-2-ium is a cationic chemical compound characterized by a triaza-dien-ium ring with a butyl group attached to the nitrogen atom. 1-(4-cyanobutyl)triaza-1,2-dien-2-ium also features a cyano group, which is a carbon and nitrogen atom triple-bonded to each other, connected to the butyl group. This unique molecular structure endows the compound with specific properties that make it suitable for various scientific and industrial applications.
Uses
Used in Coordination Chemistry:
1-(4-cyanobutyl)triaza-1,2-dien-2-ium is used as a ligand in coordination chemistry for its ability to form stable complexes with metal ions. The presence of the cyano group and the butyl chain allows for versatile coordination modes, enhancing the stability and reactivity of the resulting metal complexes.
Used in Organic Synthesis:
In the field of organic synthesis, 1-(4-cyanobutyl)triaza-1,2-dien-2-ium is used as a precursor for the synthesis of other organic compounds. Its unique structure and reactivity make it a valuable building block for creating a wide range of molecules with diverse applications, such as pharmaceuticals, agrochemicals, and advanced materials.
Used in Pharmaceutical Industry:
1-(4-cyanobutyl)triaza-1,2-dien-2-ium is used as a key intermediate in the development of new pharmaceuticals. Its unique molecular structure can be exploited to design and synthesize novel drug candidates with improved potency, selectivity, and pharmacokinetic properties.
Used in Material Science:
In the material science industry, 1-(4-cyanobutyl)triaza-1,2-dien-2-ium can be used as a component in the development of advanced materials with specific properties, such as conductivity, magnetism, or optical activity. Its incorporation into polymers, nanoparticles, or other composite materials can lead to the creation of materials with enhanced performance and novel applications.
Used in Analytical Chemistry:
1-(4-cyanobutyl)triaza-1,2-dien-2-ium can be employed as a reagent or a sensing element in analytical chemistry. Its unique chemical properties and reactivity can be utilized to develop new methods for the detection, quantification, or separation of various analytes, contributing to the advancement of analytical techniques and technologies.
Check Digit Verification of cas no
The CAS Registry Mumber 21994-41-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,9,9 and 4 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 21994-41:
(7*2)+(6*1)+(5*9)+(4*9)+(3*4)+(2*4)+(1*1)=122
122 % 10 = 2
So 21994-41-2 is a valid CAS Registry Number.
21994-41-2Relevant articles and documents
A γ-ray and dual redox-responsive supramolecular polymer constructed by a selenium containing pillar[5]arene dimer and a neutral guest
Zhou, Yujuan,Jie, Kecheng,Shi, Bingbing,Yao, Yong
, p. 11112 - 11114 (2015)
The first γ-radiation responsive linear supramolecular via pillararene-based host-guest recognition polymer was built successfully. What is more, this supramolecular polymer exhibited dual redox responsiveness.
Mild Synthesis of Pillar[4]arene[1]cis-diepoxy-p-dione and Guest-Assisted Formation of a 2D Network in the Solid State
Han, Chengyou,Dong, Shengyi,Zhao, Dezhi,Sun, Daofeng
, p. 6629 - 6632 (2017)
Herein, we developed an environmentally friendly, feasible method to synthesize pillar[4]arene[1]cis-diepoxy-p-dione. Strikingly, single-crystal X-ray analysis of pillar[4]arene[1]cis-diepoxy-p-dione and 5-chloropentanenitrile indicated a 1:2 stoichiometry to form a 2D network in the solid state.
Artificial light-harvesting supramolecular polymeric nanoparticles formed by pillar[5]arene-based host-guest interaction
Sun, Cai-Li,Peng, Hui-Qing,Niu, Li-Ya,Chen, Yu-Zhe,Wu, Li-Zhu,Tung, Chen-Ho,Yang, Qing-Zheng
supporting information, p. 1117 - 1120 (2018/02/07)
Artificial light-harvesting nanoparticles were prepared from supramolecular polymers comprised of pillar[5]arene with anthracene-derived donors and acceptors through host-guest interactions. The resulting water-dispersible nanoparticles displayed efficient energy transfer and excellent light harvesting ability in part because the steric bulk of pillar[5]arene suppressed the self-quenching of the chromophores.
Stronger host-guest binding does not necessarily give brighter particles: a case study on polymeric AIEE-tunable and size-tunable supraspheres
Xu, Linxian,Wang, Rongrong,Cui, Wei,Wang, Lingyun,Meier, Herbert,Tang, Hao,Cao, Derong
supporting information, p. 9274 - 9277 (2018/08/31)
Supraspheres were prepared from a pillar[5]arene-based linear polymer (the host) and several multitopic guests. According to host-guest binding studies in nanosystems, the optical and structural properties (fluorescence capability, density, and particle s
