1,1-Cyclobutanedicarboxylic acid, 3-phenyl-, diethyl ester is a complex organic compound with the chemical formula C16H18O4. It is a derivative of cyclobutanedicarboxylic acid, featuring a phenyl group at the 3-position and two ethyl ester groups attached to the carboxylic acid moieties. This molecule is characterized by its cyclic structure and the presence of aromatic and ester functional groups, which contribute to its unique chemical properties and potential applications in various fields, such as pharmaceuticals, materials science, and chemical research. The compound's structure and reactivity make it an interesting target for synthetic organic chemists, who may explore its potential uses in the development of new drugs, polymers, or other advanced materials.
1769-72-8
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Basic information
- Product Name: 1,1-Cyclobutanedicarboxylic acid, 3-phenyl-, diethyl ester
- Synonyms:
- CAS NO:1769-72-8
- Molecular Formula: C16H20O4
- Molecular Weight: 276.332
- EINECS: N/A
- Product Categories: N/A
- Mol File: 1769-72-8.mol
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Chemical Properties
- Melting Point: N/A
- Boiling Point: N/A
- Flash Point: N/A
- Appearance: N/A
- Density: N/A
- Refractive Index: N/A
- Storage Temp.: N/A
- Solubility: N/A
- CAS DataBase Reference: 1,1-Cyclobutanedicarboxylic acid, 3-phenyl-, diethyl ester(CAS DataBase Reference)
- NIST Chemistry Reference: 1,1-Cyclobutanedicarboxylic acid, 3-phenyl-, diethyl ester(1769-72-8)
- EPA Substance Registry System: 1,1-Cyclobutanedicarboxylic acid, 3-phenyl-, diethyl ester(1769-72-8)
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Safety Data
- Hazard Codes: N/A
- Statements: N/A
- Safety Statements: N/A
- WGK Germany:
- RTECS:
- HazardClass: N/A
- PackingGroup: N/A
- Hazardous Substances Data: 1769-72-8(Hazardous Substances Data)
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1769-72-8 Usage
Chemical structure
Cyclobutanedicarboxylic acid with a phenyl group at the 3-position and two ethyl ester groupsMolecular weight
264.32 g/molPhysical state
Colorless liquidApplications
Used in the synthesis of pharmaceuticals, agrochemicals, and other organic compoundsEster groups
Can undergo hydrolysis to form the corresponding acid or react with alcohols in esterification reactionsPhenyl group
Can participate in electrophilic aromatic substitution reactionsCyclobutanedicarboxylic acid core
Can undergo Diels-Alder reactions, hydrogenation, and other reactions involving the cyclobutane ringVersatility
Known for its ability to undergo various chemical reactions, making it a valuable building block in organic synthesisHazards
As with many organic compounds, it is important to consider potential hazards such as flammability, reactivity with other chemicals, and potential health risks when handling or using 1,1-Cyclobutanedicarboxylic acid, 3-phenyl-, diethyl ester.Check Digit Verification of cas no
The CAS Registry Mumber 1769-72-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,7,6 and 9 respectively; the second part has 2 digits, 7 and 2 respectively.Calculate Digit Verification of CAS Registry Number 1769-72:
(6*1)+(5*7)+(4*6)+(3*9)+(2*7)+(1*2)=108
108 % 10 = 8
So 1769-72-8 is a valid CAS Registry Number.
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1,1-Cyclobutanedicarboxylic acid, 3-phenyl-, diethyl ester
