108384-35-6 | 1-Cyclopentene-1-carboxylic acid, 3-oxo-, methyl ester

Packsize	Purity	Availability	Price	Discounted Price
100mg	95%	in stock	$155.00	$108.00
250mg	95%	in stock	$235.00	$164.00
1g	95%	in stock	$592.00	$414.00
5g	95%	in stock	$1,575.00	$1,102.00

Description

• Catalog Number: AE49442
• Chemical Name: 1-Cyclopentene-1-carboxylic acid, 3-oxo-, methyl ester
• CAS Number: 108384-35-6
• Molecular Formula: C7H8O3
• Molecular Weight: 140.13662000000002
• MDL Number: MFCD12828194
• SMILES: COC(=O)C1=CC(=O)CC1

Upstream Synthesis Route

Methyl 3-oxocyclopent-1-enecarboxylate is a versatile compound commonly utilized in chemical synthesis as a key building block for the creation of various organic molecules. Due to its unique structure and reactivity, this compound serves as a valuable intermediate in the synthesis of complex organic compounds.One of the prominent applications of Methyl 3-oxocyclopent-1-enecarboxylate is its role in the formation of heterocyclic compounds, particularly in the synthesis of substituted cyclopentene derivatives. By undergoing various reactions such as nucleophilic addition, condensation, and cyclization, this compound can be transformed into structurally diverse molecules with diverse functionalities.Furthermore, Methyl 3-oxocyclopent-1-enecarboxylate can also participate in Diels-Alder reactions, where it acts as a dienophile in the formation of cyclohexene derivatives. This reaction is widely employed in organic chemistry for the construction of cyclic compounds and can lead to the formation of complex polycyclic structures.In addition to its use in heterocyclic and cyclohexene synthesis, Methyl 3-oxocyclopent-1-enecarboxylate can be incorporated into multistep synthetic pathways to access a wide range of bioactive molecules, pharmaceuticals, and natural products. Its strategic placement in synthetic routes enables chemists to introduce functionality, stereochemistry, and complexity into target molecules efficiently.Overall, Methyl 3-oxocyclopent-1-enecarboxylate plays a crucial role in modern chemical synthesis by enabling the construction of diverse organic compounds with tailored properties and functionalities. Its versatility and reactivity make it a valuable tool for synthetic chemists seeking to access structurally complex molecules for various applications.