22459-57-0 Usage
Description
2,4,6-triphenyl-1,2,3,4-tetrahydro-1,2,4,5-tetrazine, also known as TAT, is a synthetic compound characterized by its tetrazine backbone. It is recognized for its high energy and reactivity, which have garnered attention in the realms of organic chemistry and materials science. TAT's capacity to engage in various chemical reactions, such as cycloaddition with strained alkenes and bioorthogonal chemistry, positions it as a versatile agent for the creation of innovative materials and bioconjugation methods. Despite its potential, the compound's energetic and reactive attributes necessitate cautious handling and storage.
Uses
Used in Organic Chemistry:
2,4,6-triphenyl-1,2,3,4-tetrahydro-1,2,4,5-tetrazine is used as a reactive intermediate for [its ability to participate in cycloaddition reactions with strained alkenes], which is crucial for the synthesis of complex organic molecules and the development of novel chemical compounds.
Used in Materials Science:
In the field of materials science, 2,4,6-triphenyl-1,2,3,4-tetrahydro-1,2,4,5-tetrazine is utilized as a building block for [the creation of new materials with unique properties], leveraging its high-energy and reactive nature to form stable and functional materials.
Used in Drug Delivery:
2,4,6-triphenyl-1,2,3,4-tetrahydro-1,2,4,5-tetrazine is employed as a component in drug delivery systems for [its potential to enhance the targeting and release of therapeutic agents], capitalizing on its reactivity to facilitate specific drug interactions and improve treatment outcomes.
Used in Bioimaging:
In bioimaging applications, 2,4,6-triphenyl-1,2,3,4-tetrahydro-1,2,4,5-tetrazine is used as a labeling agent for [its capacity to form stable covalent bonds with biological molecules], allowing for the precise tracking and visualization of cellular processes and structures.
Used in Click Chemistry:
2,4,6-triphenyl-1,2,3,4-tetrahydro-1,2,4,5-tetrazine is utilized as a reactant in click chemistry for [its role in bioorthogonal reactions], which are essential for the efficient and specific modification of biomolecules without disrupting biological systems.
Used in Polymer Synthesis:
Within polymer science, 2,4,6-triphenyl-1,2,3,4-tetrahydro-1,2,4,5-tetrazine is used as a monomer or cross-linking agent for [the synthesis of polymers with tailored properties], taking advantage of its reactivity to create materials with specific mechanical, thermal, or chemical characteristics.
Check Digit Verification of cas no
The CAS Registry Mumber 22459-57-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,4,5 and 9 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 22459-57:
(7*2)+(6*2)+(5*4)+(4*5)+(3*9)+(2*5)+(1*7)=110
110 % 10 = 0
So 22459-57-0 is a valid CAS Registry Number.
22459-57-0Relevant articles and documents
Kinetics and mechanism of monomolecular heterolysis of commercial organohalogen compounds: XXXII. Solvent effects on activation parameters of heterolysis of 1-chloro-1-methylcyclopentane. Correlation analysis of solvation effects
Dvorko,Koshchii,Prokopets,Ponomareva
, p. 1882 - 1893 (2002)
Kinetics of heterolysis of 1-chloro-1-methylcyclopentane in MeOH, BuOH, cyclohexane, i-PrOH, t-BuOH, tert-C5H11OH, γ-butyrolactone, MeCN, PhCN, PhNO2, acetone, PhCOMe, cyclohexanone, and 1,2-dichloroethane at 25-50°C were studied by the verdazyl method. Correlation analysis of solvent effects on activation parameters of the reaction in 8 protic (additionally, AcOH and CF 3CH2OH) and 8 aprotic solvents together and separately in either group of solvents was performed. In all the solvents studied, two ΔH≠-ΔS≠ compensation effects were revealed.
Triarylverdazyl radicals as promising redox-active components of rechargeable organic batteries
Burtasov, A. A.,Chernyaeva, O. Yu.,Kostryukov, S. G.,Kozlov, A. Sh.,Pryanichnikova, M. K.,Tanaseichuk, B. S.
, p. 1321 - 1328 (2020/09/07)
A novel design of electroactive components of rechargeable organic batteries based on stable verdazyl radicals bearing various substituents is proposed. 3-Positioned aromatic substituents at the verdazyl moiety affect the reduction potentials and almost do not affect the oxidation potential, while 1-positioned aromatic substituents affect contrariwise the oxidation potential of this radical without any influence on the reduction potential. The acquired electrochemical data allowed us to reveal the structure—potential relationship for the cathodic and anodic processes, which provided the design of triarylverdazyl radicals possessing record-breaking parameters of the “electrochemical gap”.
Kinetics and mechanism of monomolecular heterolysis of commercial halogenated organic compounds: XXVI. Correlation analysis of solvation effects in dehydrobromination of 1-bromo-1-methylcyclohexane and tert-butyl bromide
Dvorko,Vasil'kevich,Ponomareva,Koshchii
, p. 724 - 731 (2007/10/03)
The dehydrobromination rate of 1-bromo-1-methylcyclohexane and tert-butyl bromide increases with increasing polarity, electrophilicity, and cohesiveness of a solvent, and decreases with increasing solvent nucleophilicity and polarizability; a negative effect of nucleophilic solvation is observed.
