(5-Methoxypyridin-2-yl)methanol

Base Information

• Chemical Name: (5-Methoxypyridin-2-yl)methanol
• CAS No.: 127978-70-5
• Molecular Formula: C7H9 N O2
• Molecular Weight: 139.154
• Hs Code.: 2933399090
• DSSTox Substance ID: DTXSID20480749
• Wikidata: Q72485854
• Mol file: 127978-70-5.mol

Synonyms:(5-Methoxypyridin-2-yl)methanol;127978-70-5;(5-Methoxypyridine-2-yl)methanol;2-PYRIDINEMETHANOL, 5-METHOXY-;MFCD08235020;5-METHOXY-2-PYRIDINEMETHANOL;SCHEMBL731990;DTXSID20480749;2-Hydroxymethyl-5-methoxypyridine;YSGIZFIQWAPBLG-UHFFFAOYSA-N;(5-methoxypyridin-2-yl)-methanol;AMY10061;(5-Methoxy-pyridin-2-yl)-methanol;5-Methoxy-2-(hydroxymethyl)pyridine;AKOS006284254;CS-W006204;PB32580;AC-33335;DS-12304;SY019580;FT-0738745;EN300-130819;A889112

Chemical Property of (5-Methoxypyridin-2-yl)methanol

Chemical Property:

• Refractive Index: 1.534
• Boiling Point: 262℃
• PKA: 13.22±0.10(Predicted)
• Flash Point: 112℃
• PSA: 42.35000
• Density: 1.155
• LogP: 0.58250
• Storage Temp.: Inert atmosphere,Room Temperature
• XLogP3: 0
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 2
• Exact Mass: 139.063328530
• Heavy Atom Count: 10
• Complexity: 97.6

Purity/Quality:

97% ^*data from raw suppliers

(5-Methoxypyridin-2-yl)methanol ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: COC1=CN=C(C=C1)CO
• Uses: (5-Methoxypyridin-2-yl)methanol is used in preparation of substituted pyrrolopyridinones as HPK1 antagonists and uses thereof.

Technology Process of (5-Methoxypyridin-2-yl)methanol

There total 8 articles about (5-Methoxypyridin-2-yl)methanol which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 93.0%

2-acetoxymethyl-5-methoxypyridine (75342-32-4) → 2-hydroxymethyl-5-methoxypyridine (127978-70-5)

Guidance literature:

With water; potassium hydroxide; In methanol; for 2h; Reflux;

DOI:10.1016/j.bmc.2014.12.007

Reference yield: 90.0%

5-methoxy-2-pyridinecarboxaldehyde (22187-96-8) → 2-hydroxymethyl-5-methoxypyridine (127978-70-5)

Guidance literature:

With sodium tetrahydroborate; In methanol; at 0 ℃; for 0.166667h;

Reference yield: 78.0%

5-methoxypyridine-2-carboxylic acid methyl ester (29681-39-8) → 2-hydroxymethyl-5-methoxypyridine (127978-70-5)

Guidance literature:

With diisobutylaluminium hydride; In toluene; at -78 - 0 ℃; Inert atmosphere;

DOI:10.1016/j.tetlet.2010.10.155

upstream raw materials:

2-acetoxymethyl-5-methoxypyridine

5-methoxy-2-methylpyridine-1-oxide

5-Hydroxy-2-methylpyridine

5-methoxy-2-picoline

Downstream raw materials:

2-chloromethyl-5-methoxy-pyridine

5-methoxy-2-pyridinecarboxaldehyde

(S)-(+)-N-[(1E)-(5-methoxy-2-pyridinyl)methylidene]-4-methylbenzenesulfinamide

N-(5-(1H-imidazol-2-yl)-2-methylphenyl)-4-((5-methoxypyridin-2-yl)methoxy)benzamide