4445-58-3 Usage
General Description
[1,1'-biphenyl]-3,4-dicarboxylic acid is a chemical compound with the molecular formula C16H10O4. It is a dicarboxylic acid derivative of biphenyl, which consists of two benzene rings connected by a single carbon-carbon bond. [1,1'-biphenyl]-3,4-dicarboxylic acid is used in the synthesis of advanced organic materials and is often employed as a building block in the preparation of coordination polymers and metal-organic frameworks. Its unique structure and properties make it useful in various applications such as in the development of functional materials, pharmaceuticals, and electronic devices. Additionally, [1,1'-biphenyl]-3,4-dicarboxylic acid has potential applications in the field of supramolecular chemistry due to its ability to form non-covalent interactions with other molecules.
Check Digit Verification of cas no
The CAS Registry Mumber 4445-58-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,4,4 and 5 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 4445-58:
(6*4)+(5*4)+(4*4)+(3*5)+(2*5)+(1*8)=93
93 % 10 = 3
So 4445-58-3 is a valid CAS Registry Number.
4445-58-3Relevant articles and documents
Metallo-β-lactamase inhibitory activity of phthalic acid derivatives
Hiraiwa, Yukiko,Morinaka, Akihiro,Fukushima, Takayoshi,Kudo, Toshiaki
scheme or table, p. 5162 - 5165 (2010/03/24)
4-Butyl-3-methylphthalic acid was recognized as a metallo-β-lactamase inhibitor. The structure-activity relationship study of substituted phthalic acids afforded 3-phenylphthalic acid derivatives as potent IMP-1 inhibitors. On the other hand, 3-substituted with 4-hydroxyphenyl phthalic acid derivative displayed a potent combination effect with biapenem (BIPM) against Pseudomonas aeruginosa that produce IMP-1.
Reactive Annulenones: A Comparative Study
Gavina, Francisco,Costero, Ana M.,Gonzalez, Ana M.
, p. 2060 - 2063 (2007/10/02)
Two new and hitherto elusive annulenones, 3-phenylcyclopentadienone and bicycloocta-1(5),3,6-triene-2,8-dione, are reported.Their lifetimes and reactivities have been studied in comparison with those of the related annulenones cyclopentadienone and 4-phenylbicycloocta-1(5),3,6-triene-2,8-dione.The influence of structure and substituents on the stabilities of these species has thereby been established.