93351-55-4 Usage
Description
1,3-Dioxane-4-methanol,2-phenyl-(9CI), also known as 2-phenyl-1,3-dioxane-4-methanol, is a chemical compound belonging to the phenyldioxane class. This organic compound features a dioxane ring with a phenyl group attached to it, providing unique structural and functional properties that make it valuable in various applications.
Uses
Used in Pharmaceutical Synthesis:
1,3-Dioxane-4-methanol,2-phenyl-(9CI) is used as a key intermediate in the synthesis of pharmaceuticals for its ability to contribute to the formation of complex molecular structures. Its presence in the synthesis process can enhance the development of new drugs with improved therapeutic properties.
Used in Fine Chemicals Production:
In the fine chemicals industry, 1,3-Dioxane-4-methanol,2-phenyl-(9CI) is utilized as a building block for creating specialty chemicals with specific applications. Its unique structure allows for the production of high-quality compounds used in various sectors, including fragrances, dyes, and other specialty chemical products.
Used in Agricultural Product Development:
1,3-Dioxane-4-methanol,2-phenyl-(9CI) is employed in the development of agricultural products, such as pesticides and herbicides. Its incorporation into these products can lead to more effective and targeted solutions for crop protection, contributing to increased agricultural yields and sustainability.
Used as a Solvent in Industrial Applications:
Due to its solvent properties, 1,3-Dioxane-4-methanol,2-phenyl-(9CI) is used in various industrial applications. It serves as a versatile solvent for dissolving a wide range of substances, facilitating processes in industries such as manufacturing, chemical production, and material science. Its ability to dissolve various compounds makes it a valuable asset in these fields.
Check Digit Verification of cas no
The CAS Registry Mumber 93351-55-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,3,3,5 and 1 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 93351-55:
(7*9)+(6*3)+(5*3)+(4*5)+(3*1)+(2*5)+(1*5)=134
134 % 10 = 4
So 93351-55-4 is a valid CAS Registry Number.
93351-55-4Relevant articles and documents
Total Synthesis and Biological Evaluation of Siladenoserinol A and its Analogues
Yoshida, Masahito,Saito, Koya,Kato, Hikaru,Tsukamoto, Sachiko,Doi, Takayuki
supporting information, p. 5147 - 5150 (2018/03/26)
The total synthesis of siladenoserinol A, an inhibitor of the p53–Hdm2 interaction, has been achieved. AuCl3-catalyzed hydroalkoxylation of an alkynoate derivative smoothly and regioselectively proceeded to afford a bicycloketal in excellent yield. A glycerophosphocholine moiety was successfully introduced through the Horner–Wadsworth–Emmons reaction using an originally developed phosphonoacetate derivative. Finally, removal of the acid-labile protecting groups, followed by regioselective sulfamate formation of the serinol moiety afforded the desired siladenoserinol A, and benzoyl and desulfamated analogues were also successfully synthesized. Biological evaluation showed that the sulfamate is essential for biological activity, and modification of the acyl group on the bicycloketal can improve the inhibitory activity against the p53–Hdm2 interaction.
ANTIBACTERIAL AGENTS
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Page/Page column 131-132, (2013/12/03)
Antibacterial compounds of formula (I) are provided, as well as stereoisomers and pharmaceutically acceptable salts thereof; pharmaceutical compositions comprising such compounds; methods of treating bacterial infections by the administration of such compounds; and processes for the preparation of such compounds.
New and concise approach to (R)-α-lipoic acid
Wei, Zhen,Lan, Hong-Qiao,Zheng, Jian-Feng,Huang, Pei-Qiang
experimental part, p. 691 - 701 (2009/07/18)
A concise enantiospecific synthesis of (S)-6,8-bis(methylsulfonyloxy)- octanoic acid (2), a ready precursor of (R)-(+)-α-lipoic acid (1), is reported. The key step of the synthesis is the coupling of the tosylate derived from (R)-malic acid with phenylpro
