155818-14-7

Basic information

• Product Name: 2,2-Dimethyl-1,3-dioxane-5-carboxylic Acid Methyl Ester
• Synonyms: 2,2-Dimethyl-1,3-dioxane-5-carboxylic Acid Methyl Ester
• CAS NO: 155818-14-7
• Molecular Formula: C₈H₁₄O₄
• Molecular Weight: 174.19436
• Product Categories: Heterocycles;Intermediates;Heterocycles, Intermediates
• Mol File: 155818-14-7.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 196.8±25.0 °C(Predicted)
• Appearance: /
• Density: 1.058±0.06 g/cm3(Predicted)
• Storage Temp.: Refrigerator
• Solubility: Chloroform (Slightly), Ethyl Acetate (Slightly)
• CAS DataBase Reference: 2,2-Dimethyl-1,3-dioxane-5-carboxylic Acid Methyl Ester(CAS DataBase Reference)
• NIST Chemistry Reference: 2,2-Dimethyl-1,3-dioxane-5-carboxylic Acid Methyl Ester(155818-14-7)
• EPA Substance Registry System: 2,2-Dimethyl-1,3-dioxane-5-carboxylic Acid Methyl Ester(155818-14-7)

Safety Data

• Hazardous Substances Data: 155818-14-7(Hazardous Substances Data)

Usage

Description

2,2-Dimethyl-1,3-dioxane-5-carboxylic Acid Methyl Ester, with the CAS number 155818-14-7, is a light yellow oil compound that is primarily utilized in the field of organic synthesis. Its unique chemical structure and properties make it a valuable component in the creation of various complex organic molecules.

Uses

Used in Organic Synthesis:
2,2-Dimethyl-1,3-dioxane-5-carboxylic Acid Methyl Ester is used as a synthetic intermediate for the production of various organic compounds. Its light yellow oil consistency and unique chemical structure allow it to be a versatile building block in the synthesis of a wide range of molecules, including pharmaceuticals, agrochemicals, and specialty chemicals.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 2,2-Dimethyl-1,3-dioxane-5-carboxylic Acid Methyl Ester is used as a key component in the development of new drugs. Its unique properties enable it to be incorporated into the molecular structures of potential therapeutic agents, contributing to their overall efficacy and safety.
Used in Agrochemical Industry:
2,2-Dimethyl-1,3-dioxane-5-carboxylic Acid Methyl Ester is also employed in the agrochemical industry for the synthesis of novel pesticides and other crop protection agents. Its incorporation into these molecules can enhance their effectiveness in protecting crops from pests and diseases, ultimately contributing to increased agricultural productivity.
Used in Specialty Chemicals:
In the specialty chemicals sector, 2,2-Dimethyl-1,3-dioxane-5-carboxylic Acid Methyl Ester is used to create unique compounds with specific applications, such as additives for the plastics and coatings industries. Its versatility and compatibility with various other chemical components make it an essential ingredient in the development of high-performance specialty chemicals.

Upstream product

• 111934-93-1 2,2-Dimethyl-[1,3]dioxane-5,5-dicarboxylic acid dimethyl ester 
• 35329-73-8 dimethyl 2,2-bis(hydroxymethyl)malonate 

Downstream Products

• 4728-12-5 2,2-dimethyl-5-hydroxymethyl-1,3-dioxane 
• 179096-67-4 (2,2-Dimethyl-[1,3]dioxan-5-ylmethyl)-(1-methyl-1-phenyl-ethyl)-amine 
• 179096-68-5 N-(2,2-Dimethyl-[1,3]dioxan-5-ylmethyl)-2,5-dimethyl-N-(1-methyl-1-phenyl-ethyl)-benzamide 
• 179096-72-1 N-(1-ethylcyclopentyl)-[2-(4-{2-[(2,2-dimethyl[1,3]dioxan-5-yl)methyl](1-methyl-1-phenylethyl)carbamoyl}-4-methylphenyl)-3-hydroxybutyl]-N-(2-hydroxyethyl)benzamide 
• 1026429-40-2 2-(4-{2-[[2-(tert-Butyl-diphenyl-silanyloxy)-ethyl]-(1-ethyl-cyclopentyl)-carbamoyl]-phenyl}-2-oxo-butyl)-N-(2,2-dimethyl-[1,3]dioxan-5-ylmethyl)-5-methyl-N-(1-methyl-1-phenyl-ethyl)-benzamide 
• 1027196-80-0 2-(4-{2-[[2-(tert-Butyl-diphenyl-silanyloxy)-ethyl]-(1-ethyl-cyclopentyl)-carbamoyl]-phenyl}-2-hydroxy-butyl)-N-(2,2-dimethyl-[1,3]dioxan-5-ylmethyl)-5-methyl-N-(1-methyl-1-phenyl-ethyl)-benzamide 
• 162706-00-5 5-aminocarbonyl-2,2-dimethyl-1,3-dioxane 

Relevant articles and documents

Enzyme assisted syntheses of chiral building blocks for isosters of diglycerides, phospholipids and PAF

Lipase catalyzed desymmetrizations of suitably substituted, achiral 1,3-diols lead to the corresponding chiral building blocks of high enantiomeric purities, starting materials for the synthesis of isosteric carba-analogues of 1,2-sn-diglycerides and phospholipids with interesting biological activities. Lipase catalyzed resolutions of the corresponding ether derivatives lead to the corresponding building blocks for carba-analogues of PAF.