Cas no 1142223-06-0 ((βR)?-β-?Cyclopropyl-?3-?hydroxybenzenepropanoic Acid Methyl Ester)

(βR)-β-Cyclopropyl-3-hydroxybenzenepropanoic Acid Methyl Ester is a chiral ester derivative featuring a cyclopropyl group and a hydroxy-substituted benzene ring. Its stereospecific β-configuration enhances selectivity in synthetic applications, particularly in pharmaceutical intermediates and asymmetric synthesis. The cyclopropyl moiety contributes to structural rigidity, potentially improving metabolic stability in bioactive compounds. The methyl ester group offers versatility for further derivatization, such as hydrolysis or transesterification. This compound is valuable in medicinal chemistry research, where its defined stereochemistry and functional groups facilitate the development of targeted molecules. High purity and precise stereochemical control ensure reproducibility in complex synthetic pathways.
(βR)?-β-?Cyclopropyl-?3-?hydroxybenzenepropanoic Acid Methyl Ester structure
1142223-06-0 structure
Product Name:(βR)?-β-?Cyclopropyl-?3-?hydroxybenzenepropanoic Acid Methyl Ester
CAS No:1142223-06-0
MF:C13H16O3
MW:220.264344215393
CID:3042195
Update Time:2025-10-29

(βR)?-β-?Cyclopropyl-?3-?hydroxybenzenepropanoic Acid Methyl Ester Chemical and Physical Properties

Names and Identifiers

    • (βR)?-β-?Cyclopropyl-?3-?hydroxybenzenepropanoic Acid Methyl Ester
    • (βR)-β-Cyclopropyl-3-hydroxybenzenepropanoic Acid Methyl Ester
    • Methyl (βR)-β-cyclopropyl-3-hydroxybenzenepropanoate (ACI)
    • (βR)-β-Cyclopropyl-3-hydroxy-Benzenepropanoic acid methyl ester
    • Inchi： 1S/C13H16O3/c1-16-13(15)8-12(9-5-6-9)10-3-2-4-11(14)7-10/h2-4,7,9,12,14H,5-6,8H2,1H3/t12-/m1/s1
    • InChI Key： PXBFBXFVUPMAJK-GFCCVEGCSA-N
    • SMILES： [C@@H](C1CC1)(C1C=CC=C(O)C=1)CC(=O)OC

(βR)?-β-?Cyclopropyl-?3-?hydroxybenzenepropanoic Acid Methyl Ester Pricemore >>

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Benzenepropanoic acid, ?-cyclopropyl-3-hydroxy-, methyl ester, (?R)-
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(βR)?-β-?Cyclopropyl-?3-?hydroxybenzenepropanoic Acid Methyl Ester Production Method

Production Method 1

Reaction Conditions
Reference
Discovery of AM-1638: A Potent and Orally Bioavailable GPR40/FFA1 Full Agonist
Brown, Sean P.; Dransfield, Paul J.; Vimolratana, Marc; Jiao, XianYun; Zhu, Liusheng; et al, ACS Medicinal Chemistry Letters, 2012, 3(9), 726-730

Production Method 2

Reaction Conditions
Reference
Design and Synthesis of Novel, Selective GPR40 AgoPAMs
Plummer, Christopher W. ; Clements, Matthew J.; Chen, Helen; Rajagopalan, Murali; Josien, Hubert; et al, ACS Medicinal Chemistry Letters, 2017, 8(2), 221-226

(βR)?-β-?Cyclopropyl-?3-?hydroxybenzenepropanoic Acid Methyl Ester Raw materials

(βR)?-β-?Cyclopropyl-?3-?hydroxybenzenepropanoic Acid Methyl Ester Preparation Products

(βR)?-β-?Cyclopropyl-?3-?hydroxybenzenepropanoic Acid Methyl Ester Related Literature

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