25458-44-0 Usage
Description
4-(MethoxyMethoxy)benzoic acid, also known as methyl 4-(methoxymethoxy)benzoate, is a chemical compound that features a benzoic acid core with two methoxy groups attached to a single carbon atom. This versatile molecule is widely recognized for its applications in the chemical industry, particularly as an intermediate in the synthesis of pharmaceuticals, agrochemicals, and dyes.
Uses
Used in Pharmaceutical Industry:
4-(MethoxyMethoxy)benzoic acid is used as an intermediate for the synthesis of various pharmaceuticals, contributing to the development of new drugs and improving existing ones. Its unique structure allows for the creation of a diverse range of organic compounds, making it a valuable building block in medicinal chemistry.
Used in Agrochemical Industry:
In the agrochemical sector, 4-(MethoxyMethoxy)benzoic acid is utilized as a precursor in the production of various agrochemicals. Its role in this industry is crucial for the development of effective and environmentally friendly solutions for pest control and crop protection.
Used in Dye Industry:
4-(MethoxyMethoxy)benzoic acid is used as a starting material for the preparation of dyes, playing a significant role in the coloration of textiles, plastics, and other materials. Its versatility in chemical reactions enables the creation of a wide array of dyes with different properties and applications.
Used in Organic Synthesis:
As a reagent in organic synthesis, 4-(MethoxyMethoxy)benzoic acid is employed for the preparation of esters and other functionalized derivatives. Its structural features and properties make it a promising candidate for the development of new organic compounds with various applications.
Used in Medicinal Chemistry:
Due to its structural features and properties, 4-(MethoxyMethoxy)benzoic acid may have potential applications in the field of medicinal chemistry. Its ability to form a variety of organic compounds positions it as a valuable asset in the discovery and development of new pharmaceutical agents.
Check Digit Verification of cas no
The CAS Registry Mumber 25458-44-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,5,4,5 and 8 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 25458-44:
(7*2)+(6*5)+(5*4)+(4*5)+(3*8)+(2*4)+(1*4)=120
120 % 10 = 0
So 25458-44-0 is a valid CAS Registry Number.
25458-44-0Relevant articles and documents
First total synthesis of mariamide A
Xia, Yamu,Chen, Chenglong,Li, Mengying,Zhou, Weizeng,Sun, Shuyu,Chu, Shanpeng,Wang, Hui
, p. 114 - 120 (2020)
Mariamide A, a lignanamide isolated from the seeds of Silybum marianum, has demonstrated potential utility as an antioxidant and antidiabetic agent and possesses an 8-O-4′ neolignan skeleton. Herein, a first total synthesis of mariamide A is presented that proceeds in nine steps using vanillin as the starting material. The key steps for the preparation of mariamide A involve an I2-catalyzed bromomethoxylation of an alkene group, a nucleophilic substitution followed by a sequential elimination and a monoacylation reaction.
Discovery of deoxyceramide analogs as highly selective ACER3 inhibitors in live cells
Bielsa, Núria,Casasampere, Mireia,Aseeri, Mazen,Casas, Josefina,Delgado, Antonio,Abad, José Luis,Fabriàs, Gemma
, (2021/03/08)
Acid (AC), neutral (NC) and alkaline ceramidase 3 (ACER3) are the most ubiquitous ceramidases and their therapeutic interest as targets in cancer diseases has been well sustained. This supports the importance of discovering potent and specific inhibitors
COMPOSITIONS AND METHODS OF MODULATING SHORT-CHAIN DEHYDROGENASE ACTIVITY
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Paragraph 00576, (2020/06/10)
Compounds and methods of modulating 15-PGDH activity, modulating tissue prostaglandin levels, treating disease, diseases disorders, or conditions in which it is desired to modulate 15-PGDH activity and/or prostaglandin levels include 15-PGDH inhibitors described herein.