1142223-08-2 | Benzenepropanoic acid, beta-cyclopropyl-3-hydroxy-, methyl ester, (betas)-

Packsize	Purity	Availability	Price	Discounted Price
100mg	98%	in stock	$131.00	$92.00
250mg	98%	in stock	$254.00	$178.00
1g	98%	in stock	$323.00	$226.00
5g	98%	in stock	$1,129.00	$791.00

Description

• Catalog Number: AA13880
• Chemical Name: Benzenepropanoic acid, beta-cyclopropyl-3-hydroxy-, methyl ester, (betas)-
• CAS Number: 1142223-08-2
• Molecular Formula: C13H16O3
• Molecular Weight: 220.2643
• MDL Number: MFCD27956898
• SMILES: COC(=O)C[C@H](c1cccc(c1)O)C1CC1

Upstream Synthesis Route

The (S)-Methyl 3-cyclopropyl-3-(3-hydroxyphenyl)propanoate is a valuable reagent in chemical synthesis, renowned for its versatile applications in the field. This compound plays a crucial role in organic reactions, particularly in the formation of complex molecules with stereochemical precision. Its cyclopropyl moiety provides a unique scaffold for building diverse chemical structures, while the hydroxyphenyl group offers opportunities for further functionalization.In chemical synthesis, (S)-Methyl 3-cyclopropyl-3-(3-hydroxyphenyl)propanoate can act as a chiral building block, enabling the creation of enantiopure compounds essential in pharmaceuticals, agrochemicals, and materials science. Its cyclopropyl ring imparts rigidity and shape selectivity to the molecules it is incorporated into, influencing their biological activity and physical properties. Additionally, the hydroxyphenyl functionality can participate in hydrogen bonding and other intermolecular interactions, enhancing the specificity and reactivity of the final products.Moreover, the presence of the ester group in (S)-Methyl 3-cyclopropyl-3-(3-hydroxyphenyl)propanoate offers a handle for further derivatization, allowing for the introduction of various functional groups to tailor the compound for specific synthetic goals. This compound's ability to serve as a chiral, versatile, and modifiable building block makes it a valuable asset in the arsenal of synthetic chemists, enabling the construction of intricate molecular architectures with strategic control over stereochemistry and functionality.