1807547-39-2 Usage
Uses
Used in Polymer Production:
DIMTFA is utilized as a monomer in the synthesis of high-performance polymers and copolymers, particularly within the realms of liquid crystal and electronic materials. Its role in these applications is pivotal due to its ability to contribute to the overall stability and functionality of the resulting materials.
Used in Material Science:
As a building block, DIMTFA is employed in the synthesis of various functional materials and chemical compounds. Its presence in these materials is instrumental in enhancing their thermal and mechanical properties, which is crucial for their performance in a wide array of industrial and technological applications.
Used in Advanced Material Development:
DIMTFA is recognized for its excellent thermal and mechanical properties, making it a valuable component in the development of advanced materials. Its inclusion in these materials ensures that they can withstand high temperatures and mechanical stress, which is essential for their use in demanding environments and applications.
Check Digit Verification of cas no
The CAS Registry Mumber 1807547-39-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,8,0,7,5,4 and 7 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1807547-39:
(9*1)+(8*8)+(7*0)+(6*7)+(5*5)+(4*4)+(3*7)+(2*3)+(1*9)=192
192 % 10 = 2
So 1807547-39-2 is a valid CAS Registry Number.
1807547-39-2Relevant academic research and scientific papers
Grosjean, Sylvain,Hassan, Zahid,W?ll, Christof,Br?se, Stefan
, p. 1446 - 1460 (2019)
A modular synthesis of multi-functionalized biphenyl, terphenyl and higher linear oligophenylene dicarboxylic acids and pyridine-terminated oligoarenes by stepwise palladium–catalyzed borylation/Suzuki–Miyaura cross-coupling reactions is described. The presence of several distinct functional groups such as azide, hydroxy, and alkyne, as well as coordinative functional end groups (carboxylic acid or pyridine) combined in a single oligoarene molecular unit at strategic positions offer an advantageous dual-utility. First, these compounds can serve as useful molecular bricks (ditopic organic linkers) in the construction of complex porous crystalline materials. Second, after the assembly into the crystalline coordination networks, orthogonal functional sites within the linker-backbone offer tremendous potential from application perspectives as they can be modified by a wide range of post-synthetic modifications including azide–alkyne click chemistry. This allows further tailoring of the supramolecular assemblies to yield novel multifunctional materials.
