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3,3',5,5'-Tetrafluorobiphenyl-4,4'-dicarboxylic acid is a carboxylic acid derivative characterized by its fluorinated biphenyl structure and two carboxylic acid functional groups at the 4,4'-positions. 3,3',5,5'-tetrafluorobiphenyl-4,4'-dicarboxylic acid exhibits unique chemical properties due to the presence of fluorine atoms, which can influence its reactivity, stability, and solubility in various solvents.

31381-91-6

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31381-91-6 Usage

Uses

Used in Organic Synthesis:
3,3',5,5'-Tetrafluorobiphenyl-4,4'-dicarboxylic acid is used as an organic intermediate for the synthesis of various complex organic molecules and compounds. Its fluorinated biphenyl core and carboxylic acid groups make it a versatile building block in the preparation of pharmaceuticals, agrochemicals, and specialty chemicals.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 3,3',5,5'-tetrafluorobiphenyl-4,4'-dicarboxylic acid is used as a key intermediate in the development of new drugs. Its unique structure and properties can be exploited to design and synthesize novel drug candidates with improved pharmacological profiles, such as enhanced potency, selectivity, and bioavailability.
Used in Material Science:
3,3',5,5'-Tetrafluorobiphenyl-4,4'-dicarboxylic acid can also be utilized in material science for the creation of advanced materials with specific properties. For instance, it can be incorporated into the synthesis of polymers, coatings, and composites that exhibit enhanced thermal stability, chemical resistance, and other desirable characteristics.
Used in Chemical Research:
As a carboxylic acid derivative with a fluorinated biphenyl structure, 3,3',5,5'-tetrafluorobiphenyl-4,4'-dicarboxylic acid is a valuable compound for chemical research. It can be employed in studies aimed at understanding the effects of fluorination on molecular properties, as well as in the development of new synthetic methods and strategies for the preparation of complex organic molecules.

Check Digit Verification of cas no

The CAS Registry Mumber 31381-91-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,1,3,8 and 1 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 31381-91:
(7*3)+(6*1)+(5*3)+(4*8)+(3*1)+(2*9)+(1*1)=96
96 % 10 = 6
So 31381-91-6 is a valid CAS Registry Number.

31381-91-6Upstream product

31381-91-6Downstream Products

31381-91-6Relevant academic research and scientific papers

Fluorinated Biphenyldicarboxylate-Based Metal-Organic Framework Exhibiting Efficient Propyne/Propylene Separation

He, Chun-Ting,Li, Libo,Lin, Zhao-Ting,Liu, Qing-Yan,Wang, Yu-Ling,Yang, Ling

, (2020)

A novel fluorinated biphenyldicarboxylate ligand of 3,3′,5,5′-tetrafluorobiphenyl-4,4′-dicarboxylic acid (H2-TFBPDC) and its terbium metal-organic framework, {[Tb2(TFBPDC)3(H2O)]·4.5DMF·0.5H2O}n (denoted as JXNU-6), were synthesized. JXNU-6 exhibits a three-dimensional (3D) framework built from one-dimensional (1D) terbium carboxylate helical chains bridged by TFBPDC2- linkers. The 3D framework of JXNU-6 features 1D fluorine-lined channels. The gas adsorption experiments show that the activated JXNU-6 (JXNU-6a) displays distinct adsorption behavior for propyne (C3H4) and propylene (C3H6) gases. The effective removal of a trace amount of C3H4 from C3H6 was achieved by JXNU-6a under ambient conditions, which is demonstrated by the column-breakthrough experiments. The modeling studies show that the preferential binding sites for C3H4 are the exposed F atoms on the pore surface in 1D channels. The strong C-H···F hydrogen bonds between C3H4 molecules and F atoms of TFBPDC2- ligands dominate the host-guest interactions, which mainly account for the excellent C3H4/C3H6 separation performance of JXNU-6a. This work provides a strategy for specific recognition toward C3H4 over C3H6 through the C-H···F hydrogen bond associated with the fluorinated organic ligand.

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