29237-14-7 Usage
Uses
Used in Organic Synthesis:
[1,1'-Biphenyl]-2,2'-dicarboxaldehyde, 4,4',5,5'-tetramethoxyis utilized as a key component in organic synthesis, serving as a precursor to a variety of complex organic molecules. Its unique structure and reactivity facilitate the formation of new compounds with potential applications across various industries.
Used in Pharmaceutical Production:
In the pharmaceutical industry, [1,1'-Biphenyl]-2,2'-dicarboxaldehyde, 4,4',5,5'-tetramethoxyis employed as a building block for the development of novel drugs. Its ability to participate in multiple chemical reactions allows for the creation of a wide array of drug candidates with different therapeutic properties.
Used in Drug Development:
[1,1'-Biphenyl]-2,2'-dicarboxaldehyde, 4,4',5,5'-tetramethoxy-'s properties and reactivity make it an attractive candidate for drug development. Researchers can leverage its chemical versatility to design and synthesize new molecules with potential medicinal applications, contributing to the advancement of treatments for various diseases and conditions.
Used in Chemical Research:
[1,1'-Biphenyl]-2,2'-dicarboxaldehyde, 4,4',5,5'-tetramethoxyis also used in chemical research to study the mechanisms of various reactions and to understand the behavior of different functional groups. This knowledge can be applied to improve existing synthetic methods or to develop new ones, ultimately expanding the scope of organic chemistry and its applications.
Check Digit Verification of cas no
The CAS Registry Mumber 29237-14-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,9,2,3 and 7 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 29237-14:
(7*2)+(6*9)+(5*2)+(4*3)+(3*7)+(2*1)+(1*4)=117
117 % 10 = 7
So 29237-14-7 is a valid CAS Registry Number.
29237-14-7Relevant academic research and scientific papers
Intramolecular carbonyl-ene reactions in the synthesis of peri-oxygenated hydroaromatics
Basak, Shyam,Mal, Dipakranjan
, p. 1758 - 1772 (2018/03/29)
2-Methallyl aromatic aldehydes, synthesized by Suzuki coupling of 2-formylphenylboronic acids, are shown to provide cycloalkylidene ene products under acidic conditions. Susceptibility of the products to aromatization is manoeuvred by varying the reaction conditions and catalysts including binol-derived Br?nsted acid catalysts. A peri-effect is identified as a controlling factor for the aromatizations. Several oxidative transformations of an ene product are carried out as model studies of hydroaromatic polyketide natural products.
Lignanes. 17. Recherches sur la Synthese Totale d'un Norcycloneolignane, la Metasequirine-B
Sanceau, Jean-Yves,Dhal, Robert,Brown, Eric
, p. 3363 - 3380 (2007/10/02)
The total synthesis of the racemic furano bisbenzocycloheptene 3 is described.The compound 3, which contains five asymmetric centres, is the 5,8-bis-epimer of the tetra-O-methyl derivative of metasequirin-B (1), a norcycloneolignan of unusual structure.
