15795-54-7

Basic information

• Product Name: 5-[(4-METHOXYPHENYL)METHYLENE]-2,2-DIMETHYL-1,3-DIOXANE-4,6-DIONE
• Synonyms: 5-[(4-METHOXYPHENYL)METHYLENE]-2,2-DIMETHYL-1,3-DIOXANE-4,6-DIONE;AURORA 2058;5-[(4-methoxyphenyl)methylidene]-2,2-dimethyl-1,3-dioxane-4,6-dione
• CAS NO: 15795-54-7
• Molecular Formula: C₁₄H₁₄O₅
• Molecular Weight: 262.26
• Mol File: 15795-54-7.mol
• Article Data: 59

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 5-[(4-METHOXYPHENYL)METHYLENE]-2,2-DIMETHYL-1,3-DIOXANE-4,6-DIONE(CAS DataBase Reference)
• NIST Chemistry Reference: 5-[(4-METHOXYPHENYL)METHYLENE]-2,2-DIMETHYL-1,3-DIOXANE-4,6-DIONE(15795-54-7)
• EPA Substance Registry System: 5-[(4-METHOXYPHENYL)METHYLENE]-2,2-DIMETHYL-1,3-DIOXANE-4,6-DIONE(15795-54-7)

Safety Data

• Hazardous Substances Data: 15795-54-7(Hazardous Substances Data)

Usage

Description

5-[(4-Methoxyphenyl)methylene]-2,2-dimethyl-1,3-dioxane-4,6-dione is a chemical compound with the molecular formula C15H16O5. It is a dioxane derivative containing a methoxyphenyl group and a dimethyl group, along with a dione functional group. 5-[(4-METHOXYPHENYL)METHYLENE]-2,2-DIMETHYL-1,3-DIOXANE-4,6-DIONE has potential applications in the field of organic chemistry, specifically in the synthesis of pharmaceuticals and agrochemicals. Its unique structure and properties make it a valuable building block for the creation of new molecules with desired biological or chemical activities.

Uses

Used in Pharmaceutical Industry:
5-[(4-Methoxyphenyl)methylene]-2,2-dimethyl-1,3-dioxane-4,6-dione is used as a building block for the synthesis of pharmaceuticals. Its unique structure allows for the creation of new molecules with potential therapeutic applications.
Used in Agrochemical Industry:
5-[(4-Methoxyphenyl)methylene]-2,2-dimethyl-1,3-dioxane-4,6-dione is used as a building block for the synthesis of agrochemicals. Its properties can be utilized to develop new compounds with agricultural applications, such as pesticides or herbicides.
Used in Organic Chemistry Research:
5-[(4-Methoxyphenyl)methylene]-2,2-dimethyl-1,3-dioxane-4,6-dione is used as a research compound in the field of organic chemistry. Its structure and properties can be studied to understand its reactivity and potential use in the synthesis of other complex molecules. Further research and testing may reveal the full potential of this compound in various applications.

Upstream product

• 2033-24-1 cycl-isopropylidene malonate 
• 123-11-5 4-methoxy-benzaldehyde 
• 670-54-2 ethenetetracarbonitrile 
• 67-64-1 acetone 
• 1214-54-6 5-benzylidene Meldrum's acid 
• 622-72-0 N-(4-methoxylbenzylidene)benzylamine 
• 61958-46-1 5-(4-methoxybenzyl)-2,2-dimethyl[1,3]dioxane-4,6-dione 
• 341-02-6 trityl tetrafluoroborate 
• 1650-48-2 tris(4-methylphenyl)methylium tetrafluoroborate 
• 437-30-9 4,4',4-trimethoxytrityl tetrafluoroborate 
• 1995-50-2 (4-dimethylaminophenyl)diphenylmethylium tetrafluoroborate 
• 3585-93-1 N-(4-methoxybenzylidene)aniline oxide 
• 123-08-0 4-hydroxy-benzaldehyde 
• 108-99-6 3-Methylpyridine 

Downstream Products

• 88220-96-6 (4S,5S)-4-Acetyl-5-(4-methoxy-phenyl)-dihydro-furan-2-one 
• 73372-67-5 C₁₉H₂₅NO₅ 
• 1011710-35-2 ethyl 2-((2,2-dimethyl-4,6-dioxo-1,3-dioxan-5-yl)(4-methoxyphenyl)methyl)-3-oxobutanoate 
• 1011710-36-3 5-[2-acetyl-1-(4-methoxyphenyl)-3-oxobutyl]-2,2-dimethyl-1,3-dioxane-4,6-dione 
• 1011710-34-1 C₁₇H₁₆N₂O₅ 
• 1011710-37-4 C₂₂H₂₅O₇^(1-)*K⁽¹⁺⁾ 
• 1011710-32-9 C₂₁H₂₅O₉^(1-)*K⁽¹⁺⁾ 
• 1169681-84-8 4,4,4-trifluoro-3-(4-methoxyphenyl)butan-1-ol 

Relevant articles and documents

Synthesis and crystal structure of 5-(4-methoxybenzylidene)-2,2-dimethyl-1, 3-dioxane-4,6-dione

A new Meldrum's acid compound 5-(4-methoxybenzylidene)-2,2-dimethyl-1,3- dioxane-4,6-dione was prepared by 2,2-dimethyl-1,3-dioxane- 4,6-dione with 4-methoxybenzaldehyde in ethanol and its crystal structure was determined by X-ray crystallographic techniq

Synthesis, crystal structure and molecular modeling (AM1) of two 5-arylidene derivatives of Meldrum's acid

The synthesis and structural characterization of two 5-Arylidene derivatives of Meldrum's acid (2,2-dimethyl-1,3-dioxane-4,6-dione) are described: 5-(4-Nitrobenciliden)-2,2-dimethyl-1,3-dioxane-4,6-dione (3a), and 5-(4-Methoxybenciliden)-2,2-dimethyl-1,3-

Clean synthesis in water. Part 2: Uncatalysed condensation reaction of Meldrum's acid and aldehydes

The environment-friendly condensation of Meldrum's acid and aromatic, heteroaromatic and hindered aliphatic aldehydes is performed carrying out the reaction in water at 75°C for 2 h, avoiding the addition of any catalyst.

Enantioselective Ammonium Ylide Mediated One-Pot Synthesis of Highly Substituted γ-Butyrolactones

An ammonium ylide mediated access towards trans-β,γ-disubstituted, all-trans-α,β,γ-trisubstituted, and α,α,β,γ-tetrasubstituted γ-butyrolactones bearing a broad variety of functionalities was developed. Starting from widely accessible benzylidene Meldrum's acid derivatives and α-bromo carbonyl compounds, γ-butyrolactones were obtained in yields between 32–99% with up to excellent diastereoselectivities (>95:5) via a DABCO-mediated [2+1] annulation. Utilization of enantiomerically pure cinchona alkaloid derivatives enables the first asymmetric ammonium ylide mediated method to provide (3R,?4R)-β,γ-disubstituted and (2R,?3R,?4R)-α,β,γ-trisubstituted γ-butyrolactones in moderate to good yields with up to very good enantiomeric ratios (97:3). The scalability of the transformation was proven while determining the absolute configuration. (Figure presented.).

An alternative, practical, and ecological protocol for synthesis of arylidene analogues of Meldrum’s acid as useful intermediates

This paper presents an ecological protocol for Knoevenagel condensation using a catalytic amount of 4,4′-trimethylenedipiperidine as a versatile, efficient, safe, commercially available, inexpensive, and recyclable organocatalyst by a ball-milling process