65109-45-7 Usage
Description
2,5-dinitroterephthalic acid is a chemical compound characterized by the molecular formula C8H4N2O8. It is a yellow crystalline solid known for its role in the synthesis of organic compounds and dyes. 2,5-dinitroterephthalic acid is frequently utilized in the production of metal-organic frameworks and has garnered interest for its potential applications in pharmaceuticals and as a building block for supramolecular chemistry. Its distinctive structure and properties render it a valuable asset in a variety of chemical processes and research applications. However, due to its potential hazards and toxicity, careful handling and usage are paramount.
Uses
Used in Chemical Synthesis:
2,5-dinitroterephthalic acid is used as a key intermediate in the synthesis of various organic compounds and dyes. Its unique structure allows for versatile chemical reactions, making it a valuable component in the creation of a wide range of products.
Used in Metal-Organic Frameworks (MOFs) Production:
In the field of materials science, 2,5-dinitroterephthalic acid is employed as a building block for the development of metal-organic frameworks. These MOFs are porous materials with potential applications in gas storage, catalysis, and drug delivery due to their high surface area and tunable properties.
Used in Pharmaceutical Research:
2,5-dinitroterephthalic acid is utilized as a starting material or a structural component in the research and development of new pharmaceuticals. Its chemical properties make it a promising candidate for the creation of novel drug molecules.
Used in Supramolecular Chemistry:
As a component in supramolecular chemistry, 2,5-dinitroterephthalic acid is used to construct complex molecular systems. Its ability to form non-covalent interactions with other molecules allows for the development of self-assembling structures with potential applications in nanotechnology and molecular machines.
Used in Research Applications:
In academic and industrial research settings, 2,5-dinitroterephthalic acid is employed as a tool to study various chemical processes and reactions. Its unique properties make it an important compound for understanding and advancing the field of chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 65109-45-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,1,0 and 9 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 65109-45:
(7*6)+(6*5)+(5*1)+(4*0)+(3*9)+(2*4)+(1*5)=117
117 % 10 = 7
So 65109-45-7 is a valid CAS Registry Number.
65109-45-7Relevant articles and documents
Flexibility in metal-organic frameworks derived from positional and electronic effects of functional groups
Ha, Hyeonbin,Hahm, Hyungwoo,Jwa, Dong Gyun,Yoo, Kwangho,Park, Myung Hwan,Yoon, Minyoung,Kim, Youngjo,Kim, Min
, p. 5361 - 5368 (2017/09/26)
The position of identical functional groups and the subsequent electron density of structural benzene rings in a zinc-based metal-organic framework (MOF) have been controlled to reveal flexibility (or breathing behavior) differences. Both ortho- and para-positioned bi-functional benzene-1,4-dicarboxylic acid (BDC) ligands were synthesized with amino-, chloro-, methoxy-, and nitro groups. Additionally, two tri-functionalized, dimethoxy-amino and dimethoxy-nitro BDCs were prepared. All bi- and tri-functionalized BDCs were successfully incorporated into DABCO MOFs (DMOFs), except two diamino BDCs which were insoluble and thermally unstable. Among the eight bi-/tri-functionalized DMOFs, only para-dimethoxy exhibited flexibility in its framework after evacuation in preparation for N2 isotherm measurement. Since the dimethoxy combination has the most electron-rich environment in the benzene ring of the BDC in this series, this indicates that electron density plays a role in the flexibility changes of identically bi-functionalized DMOFs. However, the electron density alone could not fully explain the flexibility changes suggesting that the position of the functional groups is also important. These findings have been corroborated through the synthesis of two tri-functionalized DMOFs with identical functional group locations but opposite electronic environments.
Towards the development of non-enediyne approaches for mimicking enediyne chemistry: Design, synthesis and activity of a 1,4-bisdiazonium compound
Arya, Dev P.,Jebaratnam, David J.
, p. 4369 - 4372 (2007/10/02)
1,4-bisdiazonium compounds, whichmay be precursors of aryl 1,4-diradicals, have the potential to mimic the DNA cleaving activity of the enediyne antibiotics. To this end, the ability to generate and activate 1,4-bisdiazonium compounds in good yield (e.g.,
