90560-22-8 Usage
Description
5-Methoxyisophthalic acid, a derivative of isophthalic acid, is a chemical compound characterized by the molecular formula C9H8O5. It features a methoxy group attached to the aromatic ring at the 5-position, which endows it with unique structural and functional properties. As a white crystalline solid, it is sparingly soluble in water and is primarily synthesized through chemical processes. Its versatility and valuable properties make it a key building block in the creation of a wide range of organic compounds and materials, including polymers, pharmaceuticals, and electronic materials.
Uses
Used in Chemical Synthesis:
5-Methoxyisophthalic acid is used as a building block for the synthesis of various organic compounds and materials. Its unique structure allows it to be a key component in the development of new polymers, pharmaceuticals, and electronic materials, contributing to the advancement of these fields.
Used in Material Production:
In the material production industry, 5-Methoxyisophthalic acid is utilized as a precursor in the synthesis of novel materials. Its incorporation into these materials can enhance their properties, such as stability, reactivity, or conductivity, depending on the specific application.
Used in Pharmaceutical Development:
5-Methoxyisophthalic acid is used as a precursor in the synthesis of biologically active compounds. Its unique chemical structure makes it a promising candidate for the development of new pharmaceuticals, potentially leading to the creation of innovative treatments and therapies.
Used in Electronic Material Synthesis:
In the electronics industry, 5-Methoxyisophthalic acid is employed in the synthesis of electronic materials. Its properties may contribute to the development of advanced electronic components or devices, such as sensors, transistors, or other integrated circuits, by enhancing their performance or functionality.
Overall, 5-Methoxyisophthalic acid's diverse applications across various industries highlight its importance as a versatile and valuable chemical compound in modern science and technology.
Check Digit Verification of cas no
The CAS Registry Mumber 90560-22-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,5,6 and 0 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 90560-22:
(7*9)+(6*0)+(5*5)+(4*6)+(3*0)+(2*2)+(1*2)=118
118 % 10 = 8
So 90560-22-8 is a valid CAS Registry Number.
90560-22-8Relevant articles and documents
AMINOGUANIDINE HYDRAZONES AS RETROMER STABILIZERS USEFUL FOR TREATING NEUROLOGICAL DISEASES
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Page/Page column 21; 46; 50-52, (2020/10/20)
The present invention relates to novel aminoguanidine hydrazone-derivatives of Formula (I) which are effective as retromer stabilizers and useful as neuroprotecting drugs. The invention also relates to pharmaceutical compositions comprising the compounds and their use in therapy and diagnostic.
Versatile syntheses of optically pure pce pincer ligands: Facile modifications of the pendant arms and ligand backbones
Yang, Xiang-Yuan,Tay, Wee Shan,Li, Yongxin,Pullarkat, Sumod A.,Leung, Pak-Hing
supporting information, p. 1582 - 1588 (2015/05/13)
A series of chiral C-stereogenic PCP and PCN ligand precursors were prepared in situ from inexpensive achiral starting materials via a simple catalytic asymmetric P-H addition reaction in good overall yields. This facile catalytic method of preparing the ligand backbones renders easy and economical modifications of the electronically crucial para-substituent, chiral functionalities, and donor atoms for different transition metal ions. A one-pot synthetic procedure was used efficiently to prepare the corresponding optically pure pincer complexes. All the new complexes were characterized by NMR and mass spectroscopy. The molecular structures of several selected complexes have also been elucidated by X-ray crystallography. Preliminary studies indicated that minor structural changes on these novel pincer complexes affect their chemical properties significantly when they were applied as catalysts for the reaction between diphenylphosphine and chalcone.
Double Wittig reactions with 4-carboxybutylidene triphenylphosphorane as the key step in the synthesis of benzene derivatives metadisubstituted with ωω'-difunctionalized six-carbon chains
Provent, Christophe,Chautemps, Pierre,Gellon, Gisele,Pierre, Jean-Louis
, p. 1393 - 1396 (2007/10/03)
Using a double Wittig reaction from diformylbenzene derivatives, a direct synthetic way to 1,3-di(5-carboxypent-1-yl)benzene compounds is discussed.
