structure of (2-Isobutylpyridin-3-yl)methanol

(2-Isobutylpyridin-3-yl)methanol

CAS No.: 1030829-24-3
M. Wt: 165.23
M. Fa: C10H15NO
InChI Key: HIEINLRZXMTSEU-UHFFFAOYSA-N

Names and Identifiers of (2-Isobutylpyridin-3-yl)methanol

CAS Number

1030829-24-3

MDL Number

MFCD18802823

IUPAC Name

[2-(2-methylpropyl)pyridin-3-yl]methanol

InChI

InChI=1S/C10H15NO/c1-8(2)6-10-9(7-12)4-3-5-11-10/h3-5,8,12H,6-7H2,1-2H3

InChIKey

HIEINLRZXMTSEU-UHFFFAOYSA-N

Canonical SMILES

CC(C)CC1=C(C=CC=N1)CO

UNSPSC Code

12352100

Physical and chemical properties of (2-Isobutylpyridin-3-yl)methanol

Molecular Formula

C10H15NO

Molecular Weight

165.23

Safety Information of (2-Isobutylpyridin-3-yl)methanol

Pictograms

Signal Word

Warning

Safety Data Sheet

Supports customized editing of SDS information and downloading in PDF documents.

Applications of (2-Isobutylpyridin-3-yl)methanol

(2-Isobutylpyridin-3-yl)methanol has potential applications in various fields:

  • Pharmaceuticals: Its anti-inflammatory properties make it a candidate for drug development targeting inflammatory diseases.
  • Agrochemicals: Similar compounds are often explored for their herbicidal or fungicidal activities.
  • Materials Science: The compound may serve as a building block in creating novel materials with specific electronic or optical properties.

Interaction Studies of (2-Isobutylpyridin-3-yl)methanol

Interaction studies involving (2-Isobutylpyridin-3-yl)methanol focus on its binding affinity to various biological targets. For instance, studies have indicated its potential as a ligand for certain receptors or enzymes, which could lead to therapeutic applications. Investigations into its pharmacokinetics reveal that it is likely to penetrate biological membranes effectively, suggesting good bioavailability .

Biological Activity of (2-Isobutylpyridin-3-yl)methanol

Research indicates that (2-Isobutylpyridin-3-yl)methanol exhibits notable biological activities, particularly in anti-inflammatory and analgesic domains. The compound's structure suggests potential interactions with biological targets such as enzymes involved in inflammatory pathways. Preliminary studies have shown that derivatives of pyridine compounds can inhibit cyclooxygenase enzymes (COX-1 and COX-2), which are key players in inflammation and pain responses .

Retrosynthesis analysis of (2-Isobutylpyridin-3-yl)methanol

  • Route#1

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