815588-08-0

Basic information

• Product Name: 1,3-Dioxane-4-aceticacid,6-ethenyl-2,2-dimethyl-,ethylester,(4R,6S)-(9CI)
• Synonyms: 1,3-Dioxane-4-aceticacid,6-ethenyl-2,2-dimethyl-,ethylester,(4R,6S)-(9CI)
• CAS NO: 815588-08-0
• Molecular Formula: C₁₂H₂₀O₄
• Molecular Weight: 0
• Product Categories: METHYL
• Mol File: 815588-08-0.mol

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 1,3-Dioxane-4-aceticacid,6-ethenyl-2,2-dimethyl-,ethylester,(4R,6S)-(9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: 1,3-Dioxane-4-aceticacid,6-ethenyl-2,2-dimethyl-,ethylester,(4R,6S)-(9CI)(815588-08-0)
• EPA Substance Registry System: 1,3-Dioxane-4-aceticacid,6-ethenyl-2,2-dimethyl-,ethylester,(4R,6S)-(9CI)(815588-08-0)

Safety Data

• Hazardous Substances Data: 815588-08-0(Hazardous Substances Data)

Usage

Molecular Weight

208.24 g/mol

Explanation

The molecular weight is the sum of the atomic weights of all the atoms in the molecule. For 1,3-Dioxane-4-aceticacid,6-ethenyl-2,2-dimethyl-,ethylester,(4R,6S)-(9CI), it is approximately 208.24 grams per mole.

Explanation

The IUPAC name provides a systematic way to name chemical compounds based on their structure. This name indicates the presence of a 1,3-dioxane ring, a 4-acetic acid group, an ethenyl group, a 2,2-dimethyl substituent, and an ethyl ester group.

Explanation

The stereochemistry refers to the spatial arrangement of atoms in a molecule. In this case, the (4R,6S)-configuration indicates the specific arrangement of the ethenyl group and the 2,2-dimethyl substituent in the molecule.

Explanation

These are the key functional groups present in the molecule, which contribute to its chemical properties and reactivity.

Explanation

The compound is expected to dissolve in organic solvents due to its nonpolar nature and the presence of the ester functional group.

Explanation

The compound is generally stable at room temperature and pressure, but it may decompose or react under extreme conditions, such as high temperatures or exposure to strong acids or bases.

Explanation

The compound is used as a starting material or intermediate in the synthesis of various organic compounds, including pharmaceuticals and agrochemicals.

Explanation

Due to its unique structure and properties, the compound may have potential applications in the development of new drugs, agrochemicals, or materials with specific properties.

Explanation

The specific properties, reactivity, and potential applications of 1,3-Dioxane-4-aceticacid,6-ethenyl-2,2-dimethyl-,ethylester,(4R,6S)-(9CI) may require additional research to fully understand its potential and optimize its use in various fields.

Stereochemistry

(4R,6S)-configuration

Functional Groups

Ester, Dioxane ring, Acetic acid, Ethenyl group, Dimethyl substituent

Solubility

Soluble in organic solvents like ethanol, methanol, and dichloromethane

Stability

Stable under normal conditions

Applications

Organic synthesis, pharmaceuticals, agrochemicals

Potential Applications

Medicine, agriculture, materials science

Further Investigation

Properties and uses warrant further research

Upstream product

• 77-76-9 2,2-dimethoxy-propane 
• 521315-83-3 ethyl (3R,5S)-5-{[1-(tert-butyl)-1,1-dimethylsilyl]oxy}-3-hydroxy-6-heptenoate 
• 154703-69-2 ethyl (3R,5S)-3,5-isopropylidenedioxy-6-heptynoate 

Downstream Products

• 869961-63-7 ethyl 2-((4R,6S)-6-((E)-2-(5-sec-butyl-3-(4-fluorophenyl)-1-(2-(phenylamino)pyridine-4-yl)-1H-pyrazol-4-yl)vinyl)-2,2-dimethyl-1,3-dioxan-4-yl)acetate 
• 869961-74-0 ethyl 2-((4R,6S)-6-((E)-2-(3,5-diphenyl-1-(2-(phenylamino)pyrimidin-4-yl)-1H-pyrazol-4-yl)vinyl)-2,2-dimethyl-1,3-dioxan-4-yl)acetate 
• 869961-86-4 ethyl 2-((4R,6S)-6-((E)-2-(3-isopropyl-1-(2-methoxypyrimidin-4-yl)-5-(3-(trifluoromethyl)phenyl)-1H-pyrazol-4-yl)vinyl)-2,2-dimethyl-1,3-dioxan-4-yl)acetate 
• 869961-96-6 ethyl 2-((4R,6S)-2,2-dimethyl-6-((E)-2-(1-(2-(phenylamino)pyrimidin-4-yl)-5-(3-(trifluoromethyl)phenyl)-1H-pyrazol-4-yl)vinyl)-1,3-dioxan-4-yl)acetate 
• 815588-11-5 (4S,6S)-4-{2-[(2S,4S)-4,6-Bis-(tert-butyl-dimethyl-silanyloxy)-2-(4-methoxy-benzyloxy)-hexyl]-[1,3]dithian-2-ylmethyl}-6-[2-(4-methoxy-benzyloxy)-ethyl]-2,2-dimethyl-[1,3]dioxane 
• 815588-12-6 (4S,6S)-6,8-Bis-(tert-butyl-dimethyl-silanyloxy)-4-(4-methoxy-benzyloxy)-1-{(4S,6S)-6-[2-(4-methoxy-benzyloxy)-ethyl]-2,2-dimethyl-[1,3]dioxan-4-yl}-octan-2-one 
• 815588-00-2 (4S,6S)-4-Iodomethyl-6-[2-(4-methoxy-benzyloxy)-ethyl]-2,2-dimethyl-[1,3]dioxane 
• 815588-10-4 {(4S,6S)-6-[2-(4-Methoxy-benzyloxy)-ethyl]-2,2-dimethyl-[1,3]dioxan-4-yl}-methanol 
• 815588-09-1 (4S,6S)-4-[2-(4-Methoxy-benzyloxy)-ethyl]-2,2-dimethyl-6-vinyl-[1,3]dioxane 
• 627536-90-7 (4S,6S)-4-[1,3]Dithian-2-ylmethyl-6-[2-(4-methoxy-benzyloxy)-ethyl]-2,2-dimethyl-[1,3]dioxane 

Relevant articles and documents

Synthesis of AB and CD spiroketal of spongistatin 1

The AB (C1-C13) and CD (C17-C 29) spiroketal of spongistatin 1 were prepared diastereoselectively from syn- and anti-3,5-dihydroxy-6-heptenoate derived from 2-deoxy-D-ribose.