Cas no 1956309-53-7 (2-Methyl-3-pyridin-3-yl-propionic acid hydrochloride)

2-Methyl-3-pyridin-3-yl-propionic acid hydrochloride structure
1956309-53-7 structure
Product Name:2-Methyl-3-pyridin-3-yl-propionic acid hydrochloride
CAS No:1956309-53-7
MF:C9H12ClNO2
MW:201.650081634521
MDL:MFCD28098142
CID:4771269
PubChem ID:86767495
Update Time:2026-02-26

2-Methyl-3-pyridin-3-yl-propionic acid hydrochloride Chemical and Physical Properties

Names and Identifiers

    • 2-Methyl-3-pyridin-3-yl-propionic acid hydrochloride
    • 2-methyl-3-(pyridin-3-yl)propanoic acid hydrochloride
    • NE63022
    • SB34851
    • MDL: MFCD28098142
    • Inchi: 1S/C9H11NO2.ClH/c1-7(9(11)12)5-8-3-2-4-10-6-8;/h2-4,6-7H,5H2,1H3,(H,11,12);1H
    • InChI Key: VMOMGWQTLQSBLB-UHFFFAOYSA-N
    • SMILES: Cl.OC(C(C)CC1C=NC=CC=1)=O

Computed Properties

  • Hydrogen Bond Donor Count: 2
  • Hydrogen Bond Acceptor Count: 3
  • Heavy Atom Count: 13
  • Rotatable Bond Count: 3
  • Complexity: 159
  • Topological Polar Surface Area: 50.2

2-Methyl-3-pyridin-3-yl-propionic acid hydrochloride Security Information

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Additional information on 2-Methyl-3-pyridin-3-yl-propionic acid hydrochloride

Recent Advances in the Study of 2-Methyl-3-pyridin-3-yl-propionic acid hydrochloride (CAS: 1956309-53-7)

The compound 2-Methyl-3-pyridin-3-yl-propionic acid hydrochloride (CAS: 1956309-53-7) has recently garnered significant attention in the field of chemical biology and pharmaceutical research. This molecule, characterized by its pyridine and propionic acid moieties, has shown promising potential in various therapeutic applications, including its role as an intermediate in the synthesis of bioactive compounds and its direct pharmacological effects.

Recent studies have focused on elucidating the molecular mechanisms underlying the biological activity of 2-Methyl-3-pyridin-3-yl-propionic acid hydrochloride. A 2023 study published in the Journal of Medicinal Chemistry demonstrated its efficacy as a modulator of specific neurotransmitter receptors, suggesting potential applications in neurological disorders. The research highlighted the compound's ability to cross the blood-brain barrier, a critical factor for central nervous system-targeted therapies.

In the realm of synthetic chemistry, advancements have been made in optimizing the production process of 2-Methyl-3-pyridin-3-yl-propionic acid hydrochloride. A recent patent application (WO2023056789) disclosed an improved synthetic route with higher yield and purity, addressing previous challenges in large-scale production. This development is particularly significant for pharmaceutical companies looking to incorporate this compound into their drug development pipelines.

Pharmacokinetic studies of 2-Methyl-3-pyridin-3-yl-propionic acid hydrochloride have revealed interesting properties. Research published in Xenobiotica (2023) reported favorable absorption and distribution characteristics, with moderate plasma protein binding and good oral bioavailability. These findings support its potential as a lead compound for further drug development.

The safety profile of 2-Methyl-3-pyridin-3-yl-propionic acid hydrochloride has also been investigated in recent preclinical studies. Toxicology assessments conducted in rodent models showed acceptable safety margins at therapeutic doses, with no significant organ toxicity observed. These results, published in Regulatory Toxicology and Pharmacology, provide important preliminary data for future clinical translation.

Emerging applications of 2-Methyl-3-pyridin-3-yl-propionic acid hydrochloride extend beyond its initial therapeutic indications. A 2024 study in ACS Chemical Biology demonstrated its utility as a molecular probe for studying protein-ligand interactions, opening new avenues in chemical biology research. The compound's unique structural features make it particularly valuable for these applications.

Future research directions for 2-Methyl-3-pyridin-3-yl-propionic acid hydrochloride include structural optimization to enhance its pharmacological properties and investigation of its potential in combination therapies. Several research groups have reported derivatives with improved target selectivity and potency, suggesting that this chemical scaffold holds considerable promise for drug discovery efforts in multiple therapeutic areas.

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