11053-21-7 | 2-Methyl-2-butenoic acid [1,2,3,3a,4,7,8,8a-octahydro-8a-hydroxy-3a,6-dimethyl-1-isopropyl-3-oxoazulen-4-yl] ester

Availability
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Description

• Catalog Number: AE55514
• Chemical Name: 2-Methyl-2-butenoic acid [1,2,3,3a,4,7,8,8a-octahydro-8a-hydroxy-3a,6-dimethyl-1-isopropyl-3-oxoazulen-4-yl] ester
• CAS Number: 11053-21-7
• Molecular Formula: C20H30O4
• Molecular Weight: 334.4498
• SMILES: C/C=C(\C(=O)O[C@H]1C=C(C)CC[C@@]2([C@]1(C)C(=O)C[C@@H]2C(C)C)O)/C

Upstream Synthesis Route

Crispanone, a powerful chemical reagent, holds significant importance in various chemical synthesis processes. Due to its unique molecular structure and properties, Crispanone has found wide applications in organic chemistry, particularly in the field of natural product synthesis. Its high reactivity and selectivity make it a valuable tool for constructing complex molecular frameworks efficiently.One notable application of Crispanone is its role as a versatile dienophile in Diels-Alder reactions. This reaction, which involves the cycloaddition of a diene and a dienophile, is widely used in the synthesis of diverse organic compounds. Crispanone's ability to participate in Diels-Alder reactions allows chemists to rapidly access structurally intricate molecules with high stereoselectivity.Furthermore, Crispanone can act as an electrophilic reagent in various functional group transformations. Its electron-deficient nature makes it capable of reacting with nucleophilic species, leading to the formation of new carbon-carbon bonds. This property is particularly valuable in the construction of complex natural products and pharmaceutical intermediates.Overall, Crispanone's unique reactivity and versatility make it a valuable asset in the toolkit of synthetic chemists seeking efficient routes to target molecules. Its applications in Diels-Alder reactions and other key transformations highlight its significance in advancing the field of chemical synthesis.