3108-15-4 Usage
Uses
Used in Organic Synthesis:
2,5-dimethoxybenzenediazonium tetrafluoroborate is used as a key reagent for the synthesis of various organic compounds due to its ability to generate the diazonium ion. This ion can participate in a multitude of reactions, including coupling and substitution processes, which are essential for constructing complex molecular structures.
Used in the Formation of Carbon-Carbon Bonds:
In the field of organic chemistry, 2,5-dimethoxybenzenediazonium tetrafluoroborate is employed as a catalyst or reactant to facilitate the formation of carbon-carbon bonds. These bonds are fundamental to the structure of many organic molecules and are critical in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in the Formation of Carbon-Heteroatom Bonds:
2,5-dimethoxybenzenediazonium tetrafluoroborate is also used as a precursor in the formation of carbon-heteroatom bonds, such as those involving oxygen, nitrogen, or sulfur. These bonds are prevalent in a wide range of organic compounds and are integral to the development of novel materials and pharmaceutical agents.
Used in Medicinal Chemistry:
In the pharmaceutical industry, 2,5-dimethoxybenzenediazonium tetrafluoroborate is utilized as an intermediate in the synthesis of bioactive molecules. Its reactivity and the stability provided by the tetrafluoroborate counterion make it a suitable candidate for the development of new drugs and drug candidates.
Used in Materials Science:
2,5-dimethoxybenzenediazonium tetrafluoroborate is employed in the development of new materials with specific properties, such as conductivity, magnetism, or optical characteristics. Its role in creating carbon-based structures makes it valuable in the advancement of materials for electronics, sensors, and other high-tech applications.
Overall, the versatility of 2,5-dimethoxybenzenediazonium tetrafluoroborate in organic synthesis and its contribution to the development of new compounds across various industries highlight its significance as a synthetic reagent in modern chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 3108-15-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,1,0 and 8 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 3108-15:
(6*3)+(5*1)+(4*0)+(3*8)+(2*1)+(1*5)=54
54 % 10 = 4
So 3108-15-4 is a valid CAS Registry Number.
InChI:InChI=1/C8H9N2O2.BF4/c1-11-6-3-4-8(12-2)7(5-6)10-9;2-1(3,4)5/h3-5H,1-2H3;/q+1;-1
3108-15-4Relevant academic research and scientific papers
Direct and Versatile Synthesis of Red-Shifted Azobenzenes
Hansen, Mickel J.,Lerch, Michael M.,Szymanski, Wiktor,Feringa, Ben L.
supporting information, p. 13514 - 13518 (2016/10/21)
A straightforward synthesis of azobenzenes with bathochromically-shifted absorption bands is presented. It employs an ortho-lithiation of aromatic substrates, followed by a coupling reaction with aryldiazonium salts. The products are obtained with good to excellent yields after simple purification. Moreover, with the presented methodology, a structurally diverse panel of different azobenzenes, including unsymmetric tetra-ortho-substituted ones, can be readily obtained, which paves the way for future development of red-light-addressable azobenzene derivatives for in vivo application.
