4388-57-2 Usage
Description
2-Methyl-1,3-dioxolane-2-propanoic Acid, with the CAS number 4388-57-2, is a chemical compound that is characterized as a colorless oil. It is primarily utilized in the field of organic synthesis, playing a significant role in the creation of various chemical products and materials.
Uses
Used in Organic Synthesis:
2-Methyl-1,3-dioxolane-2-propanoic Acid is used as a synthetic building block for the development of a wide range of chemical compounds. Its unique structure and properties make it a valuable component in the synthesis of various organic molecules, contributing to the advancement of the chemical industry.
Used in Pharmaceutical Industry:
In the pharmaceutical sector, 2-Methyl-1,3-dioxolane-2-propanoic Acid serves as a key intermediate in the synthesis of numerous pharmaceutical compounds. Its versatility in organic synthesis allows for the creation of new drugs and medications, potentially leading to breakthroughs in the treatment of various diseases and medical conditions.
Used in Chemical Research:
2-Methyl-1,3-dioxolane-2-propanoic Acid is also employed as a research tool in the field of chemistry. Its properties and reactivity make it an ideal candidate for studying various chemical reactions and mechanisms, furthering our understanding of organic chemistry and its applications.
Used in Material Science:
In the realm of material science, 2-Methyl-1,3-dioxolane-2-propanoic Acid is utilized in the development of novel materials with specific properties. Its incorporation into the synthesis process can lead to the creation of materials with enhanced characteristics, such as improved strength, durability, or chemical resistance, depending on the desired application.
Check Digit Verification of cas no
The CAS Registry Mumber 4388-57-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,3,8 and 8 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 4388-57:
(6*4)+(5*3)+(4*8)+(3*8)+(2*5)+(1*7)=112
112 % 10 = 2
So 4388-57-2 is a valid CAS Registry Number.
4388-57-2Relevant articles and documents
Acid Catalyzed Competitive Esterification and Ketalization of Levulinic Acid with 1,2 and 1,3-Diols: The Effect of Heterogeneous and Homogeneous Catalysts
Amarasekara, Ananda S.,Animashaun, Moriam A.
, p. 1819 - 1824 (2016)
Abstract: Condensation reactions of levulinic acid (LA) with 1,2-ethanediol (1,2-ED), 1,2-propanediol (1,2-PD), and 1,3-propanediol (1,3-PD) were studied using Amberlyst-15 as well as p-toluenesulfonic acid catalysts in benzene under Dean–Stark conditions. In Amberlyst-15 catalyzed reactions the products are ketals and ketal-esters, whereas p-toluenesulfonic acid catalyzed reactions produce esters and ketal-esters as products. In p-toluenesulfonic acid catalyzed reactions with 1,2-ED and 1,3-PD, LA monoester product is formed as the major product after 180?min in 75 and 97?% yields respectively. Unlike the previously reported acid catalyzed ketalization of ethyl levulinate with diols, combined ketalization–esterification of LA with diols is a complex process. Graphical Abstract: [Figure not available: see fulltext.]
SUBSTITUTED FUSED[1,2]IMIDAZO[4,5-C] RING COMPOUNDS AND METHODS
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Page/Page column 104, (2008/06/13)
[1,2]Imidazo[4,5-c] ring compounds (e.g., imidazo[4,5-c]quinolines, imidazo[4,5-c]naphthyridines, and imidazo[4,5-c]pyridines) substituted with a fused ring containing an oxygen and/or nitrogen atom attached at the 1- and/or 2-position, pharmaceutical compositions containing the compounds, intermediates, methods of making the compounds, and methods of use of these compounds as immunomodulators, for inducing cytokine biosynthesis in animals and in the treatment of diseases including viral and neoplastic diseases, are disclosed.
Total synthesis of Cacalol
Garofalo, Albert W.,Litvak, Joane,Wang, Lisa,Dubenko, Larisa G.,Cooper, Raymond,Bierer, Donald E.
, p. 3369 - 3372 (2007/10/03)
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