222180-23-6 Usage
Uses
Used in Pharmaceutical Industry:
3'-Formyl[1,1'-biphenyl]-4-carboxylic acid is used as a key intermediate for the synthesis of pharmaceutical compounds due to its ability to be readily modified and incorporated into complex molecular structures. Its presence in drug molecules can contribute to desired pharmacological properties, such as increased bioavailability or specific binding affinities.
Used in Materials Industry:
In the materials industry, 3'-Formyl[1,1'-biphenyl]-4-carboxylic acid is utilized as a component in the development of novel materials with tailored properties. Its chemical structure allows for the creation of materials with improved thermal stability, mechanical strength, or specific optical characteristics, depending on the application requirements.
Used in Organic Synthesis:
3'-Formyl[1,1'-biphenyl]-4-carboxylic acid is used as a versatile building block in organic synthesis for the creation of a wide range of organic compounds. Its reactivity with various reagents and its compatibility with different synthetic routes make it a valuable precursor in the synthesis of specialty chemicals, agrochemicals, and other fine chemicals.
Used in Research and Development:
3'-Formyl[1,1'-biphenyl]-4-carboxylic acid is employed as a research compound in academic and industrial laboratories. It is used to explore new synthetic methodologies, investigate the properties of novel chemical entities, and develop new applications in various fields, including medicinal chemistry, materials science, and chemical engineering.
Check Digit Verification of cas no
The CAS Registry Mumber 222180-23-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,2,1,8 and 0 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 222180-23:
(8*2)+(7*2)+(6*2)+(5*1)+(4*8)+(3*0)+(2*2)+(1*3)=86
86 % 10 = 6
So 222180-23-6 is a valid CAS Registry Number.
222180-23-6Relevant articles and documents
HETEROCYCLIC INTEGRIN AGONISTS
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Paragraph 0234; 0236; 0265; 0266; 0275; 0277, (2018/07/29)
The present invention provides polycyclic oxothioxoimidazolidines, dioxoimidazolines, oxothioxooxazolidines, dioxooxazolidines, and related compounds, which are useful as integrin agonists. Methods for the treatment of integrin-mediated diseases such as cancer are also described.
Selectivity in the photo-Fenton and photocatalytic hydroxylation of biphenyl-4-carboxylic acid and derivatives (viz. 4-phenylsalicylic acid and 5-phenylsalicylic acid)
Hathway, Timothy,Chernyshov, Deborah Lipman,Jenks, William S.
supporting information, p. 1151 - 1156 (2013/01/09)
The selectivity of hydroxylation of the distal rings of 4-phenylbenzoic acid, 4-phenylsalicylic acid, and 5-phenylsalicylic acid were determined using partial TiO2-mediated photocatalytic degradation and photo-Fenton conditions. This separation of the binding site from the phenyl group being hydroxylated allows a less-biased evaluation. The hydroxylation regiochemistry behaves as qualitatively expected for an electrophilic reaction, given the assumption that 4-carboxyphenyl is a slightly electron-withdrawing substituent. Selectivity for hydroxylation of the distal phenyl in 4- and 5-phenylsalicylic acid is reversed, due to the reversal of the electronic demand, while adsorption to the TiO2 surface is assumed to be analogous for the two structures. Copyright
1H-INDOLE-2-CARBOXYLIC ACID DERIVATIVES USEFUL AS PPAR MODULATORS
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Page/Page column 65-66, (2008/06/13)
The present invention relates to certain indole derivatives that are modulators of PPAR, to processes for their preparation, to pharmaceutical compositions containing them and to their use in medicine.