207850-04-2

Basic information

• Product Name: 2-PHENYL-5-METHYL-1,3-DIOXANE-5-CARBOXYLIC ACID
• Synonyms: 2-PHENYL-5-METHYL-1,3-DIOXANE-5-CARBOXYLIC ACID
• CAS NO: 207850-04-2
• Molecular Formula: C₁₂H₁₄O₄
• Molecular Weight: 222.24
• Mol File: 207850-04-2.mol
• Article Data: 13

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2-PHENYL-5-METHYL-1,3-DIOXANE-5-CARBOXYLIC ACID(CAS DataBase Reference)
• NIST Chemistry Reference: 2-PHENYL-5-METHYL-1,3-DIOXANE-5-CARBOXYLIC ACID(207850-04-2)
• EPA Substance Registry System: 2-PHENYL-5-METHYL-1,3-DIOXANE-5-CARBOXYLIC ACID(207850-04-2)

Safety Data

• Hazardous Substances Data: 207850-04-2(Hazardous Substances Data)

Usage

General Description

2-PHENYL-5-METHYL-1,3-DIOXANE-5-CARBOXYLIC ACID is a chemical compound that belongs to the class of dioxane carboxylic acids. It is a white crystalline powder with a molecular formula of C11H12O4. 2-PHENYL-5-METHYL-1,3-DIOXANE-5-CARBOXYLIC ACID is often used in the pharmaceutical industry for its potential medicinal properties, such as its ability to act as a central nervous system stimulant. It also has potential applications in the field of organic synthesis. However, more research is needed to fully understand its properties and potential uses.

Upstream product

• 4767-03-7 2,2-bis(hydroxymethyl)propionic acid 
• 1125-88-8 benzaldehyde dimethyl acetal 
• 4403-72-9 phenylboronic acid 
• 100-52-7 benzaldehyde 

Downstream Products

• 6103-22-6 5-hydroxymethyl-5-methyl-2-phenyl[1,3]dioxane 
• 4270-73-9 2-methyl-2-<(benzyloxy)methyl>-1,3-propanediol 
• 1611446-27-5 C₂₄H₃₂O₁₀S₅ 
• 1131064-60-2 TSe-G₁-(OH)2 
• 1131064-56-6 TSe-G₁-(O₂Bn) 
• 1017238-30-0 C₂₂H₂₂FN₃O₇ 
• 199457-36-8 3-hydroxy-2-hydroxymethyl-2-methyl-propionic acid 4-{1,1-bis-[4-(3-hydroxy-2-hydroxymethyl-2-methyl-propionyloxy)-phenyl]-ethyl}-phenyl ester 
• 792931-46-5 5-Methyl-2-phenyl-[1,3]dioxane-5-carboxylic acid (5Z,8Z,11Z,14Z)-icosa-5,8,11,14-tetraenyl ester 
• 352708-07-7 benzylidene-2,2-bis(oxymethyl) propionic anhydride 
• 208581-63-9 C₆₅H₈₄O₂₀ 
• 208581-60-6 C₄-([G-1]Ph)4 

Relevant articles and documents

Dendrimer-like star polymers

Dendrimer-like star polymers, a novel type of molecular architecture, have been synthesized. The architecture of the new polymers resembles that of three-dimensional spherical dendrimers as well as classical star polymers. The controlled structures, based

Non-nucleosidic analogues of polyaminonucleosides and their influence on thermodynamic properties of derived oligonucleotides

The rationale for the synthesis of cationic modified nucleosides is higher expected nuclease resistance and potentially better cellular uptake due to an overall reduced negative charge based on internal charge compensation. Due to the ideal distance between cationic groups, polyamines are perfect counterions for oligodeoxyribonucleotides. We have synthesized non-nucleosidic analogues built from units that carry different diol structures instead of sugar residues and functionalized with polyamines. The non-nucleosidic analogues were attached as internal or 5′-terminal modifications in oligodeoxyribonucleotide strands. The thermodynamic studies of these polyaminooligonucleotide analogues revealed stabilizing or destabilizing effects that depend on the linker or polyamine used.

Selective monobenzylation of 2,2-bis(hydroxymethyl)propionic acid (bis-MPA) to yield an AB linear monomer and analogous linear oligomers

The synthesis of a mono-benzylated AB monomer based on bis-MPA is explored and accomplished via a three-step synthesis without column chromatography. This optimized synthesis utilizes a generic acid-catalyzed esterification of bis-MPA to the ethyl ester.