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Diphenyl biphenyl-4,4'-dicarboxylate, also known as 4,4'-(1,1'-biphenyl)diacetic acid, is an organic compound with the chemical formula C18H14O4. It is a white crystalline solid that is soluble in organic solvents such as ethanol and acetone. diphenyl biphenyl-4,4'-dicarboxylate is primarily used as a monomer in the production of high-performance polymers, particularly liquid crystal polymers (LCPs), due to its rigid and planar structure. LCPs are known for their excellent mechanical properties, thermal stability, and chemical resistance, making them suitable for applications in the electronics, automotive, and aerospace industries. Diphenyl biphenyl-4,4'-dicarboxylate is also used in the synthesis of various pharmaceuticals and other specialty chemicals.

3204-57-7

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3204-57-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3204-57-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,2,0 and 4 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 3204-57:
(6*3)+(5*2)+(4*0)+(3*4)+(2*5)+(1*7)=57
57 % 10 = 7
So 3204-57-7 is a valid CAS Registry Number.

3204-57-7Downstream Products

3204-57-7Relevant academic research and scientific papers

Synthesis of Heat-Resistant Polyester Containing Rigid Biphenyl Moiety by Palladium-Catalyzed Carbonylation-Polycondensation

Kubota, Yoshihiro,Takeuchi, Kazuhiko,Hanaoka, Taka-aki,Sugi, Yoshihiro

, p. 563 - 571 (1994)

For the purpose of synthesizing heat-resistant polyesters, the one-step synthesis of a rigid biphenyl-containing polyester from dihalobiphenyl and diol by palladium-catalyzed carbonylation-polycondensation was examined.The reaction parameters, such as the

Synthesis of aromatic esters catalyzed by palladium on charcoal: An efficient heterogeneous catalyst for alkoxycarbonylation of aryl iodides

Ramesh, Chinnasamy,Nakamura, Ryo,Kubota, Yoshihiro,Miwa, Minoru,Sugi, Yoshihiro

, p. 501 - 504 (2007/10/03)

Palladium on charcoal was found to catalyze the carbonylation of aryl iodides with various aliphatic alcohols as well as less reactive phenols to give the corresponding esters in high yield at 140°C and in the presence of carbon monoxide (1.0 MPa). The carbonylation-polycondensation of 2,7-diiodo-9,10-dihydrophenanthrene with bisphenol-A afforded high molecular weight polyarylate, poly [oxy-1,4-phenylene (1-methylethylidene)-1,4-phenyleneoxycarbonyl (9,10-dihydro-2,7-phenanthrenediyl) carbonyl].

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