3-(difluoromethoxy)cyclopentanecarboxylic acid

3-(difluoromethoxy)cyclopentanecarboxylic acid

ethyl cyclopentanecarboxylate

ethyl cyclopentanecarboxylate

5-(propan-2-ylidene)cyclopenta-1,3-diene

$200.00
CAS No.: 2175-91-9
Catalog No.: WLZ1391
Purity: 95%
MF: C8H10
MW: 106.168
Storage: 2-8 degree Celsius
SMILES: CC(=C1C=CC=C1)C
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CAS NO.: 2175-91-9; 5-(propan-2-ylidene)cyclopenta-1,3-diene. PROPERTIES: This diene features a cyclopenta-1,3-diene framework substituted with an isopropylidene group, creating a molecule with potential applications in organic synthesis and pharmaceutical research. The 5-(propan-2-ylidene)cyclopenta-1,3-diene typically appears as a colorless to pale yellow liquid with moderate solubility in common organic solvents. Its molecular structure includes a conjugated diene system that can participate in Diels-Alder reactions and other cycloaddition processes. For optimal stability and to preserve its diene integrity, this compound should be stored at 2-8 degree Celsius in an amber glass bottle under an inert atmosphere. When handling, appropriate safety measures including nitrile gloves and safety goggles are recommended. This compound is sensitive to light and may undergo polymerization upon exposure to UV radiation. In case of skin contact, wash thoroughly with soap and water; if eye contact occurs, rinse immediately and seek medical advice. APPLICATIONS: The 5-(propan-2-ylidene)cyclopenta-1,3-diene serves as a valuable building block in organic synthesis, particularly for creating complex polycyclic frameworks through cycloaddition reactions. The conjugated diene system provides a platform for Diels-Alder reactions with various dienophiles. In medicinal chemistry, this compound functions as an intermediate for developing pharmaceuticals targeting enzyme inhibitors and receptor modulators. The cyclopentadiene framework contributes to the formation of rigid, three-dimensional structures that facilitate receptor interactions. Additionally, the molecule finds utility in materials science as a monomer for creating polymers with specific optical and electronic properties. Researchers utilizing this compound can leverage its diene functionality to advance syntheses of complex molecular architectures for various applications in chemical biology and materials science.

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