2-Nonanoylpyridine

Base Information

• Chemical Name: 2-Nonanoylpyridine
• CAS No.: 143773-13-1
• Molecular Formula: C14H21NO
• Molecular Weight: 219.32300
• Hs Code.: 2933399090
• DSSTox Substance ID: DTXSID20397222
• Wikidata: Q82198378
• Mol file: 143773-13-1.mol

Synonyms:2-NONANOYLPYRIDINE;143773-13-1;1-(Pyridin-2-yl)nonan-1-one;1-pyridin-2-ylnonan-1-one;1-Nonanone, 1-(2-pyridinyl)-;MFCD00966398;2-pyridyl octyl ketone;SCHEMBL1254914;DTXSID20397222;AKOS011914486

Chemical Property of 2-Nonanoylpyridine

Chemical Property:

• Vapor Pressure: 0.000387mmHg at 25°C
• Boiling Point: 317.4oC at 760 mmHg
• Flash Point: 153.7oC
• PSA: 29.96000
• Density: 0.954g/cm3
• LogP: 4.01490
• Storage Temp.: 2-8°C
• XLogP3: 4.4
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 8
• Exact Mass: 219.162314293
• Heavy Atom Count: 16
• Complexity: 191

Purity/Quality:

98%min ^*data from raw suppliers

2-Nonanoylpyridine 97% ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CCCCCCCCC(=O)C1=CC=CC=N1

Technology Process of 2-Nonanoylpyridine

There total 7 articles about 2-Nonanoylpyridine 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:

1-(1-Ethoxy-1-pyridin-2-yl-nonyl)-1H-benzotriazole (1026384-07-5) → 2-Nonanoylpyridine (143773-13-1)

Guidance literature:

With hydrogenchloride; In tetrahydrofuran; Yield given; Ambient temperature;

DOI:10.1021/jo00128a039

Reference yield:

pyridine-2-carbaldehyde (1121-60-4) → 2-Nonanoylpyridine (143773-13-1)

Guidance literature:

Multi-step reaction with 3 steps

1: 51 percent / H₂SO₄ / ethanol; tetrahydrofuran / 1.) r.t., 3 h, 2.) reflux, 10 h

2: n-BuLi / tetrahydrofuran; cyclohexane / 1.) -78 deg C, 2.) 20 deg C, 30 min

3: aq. HCl / tetrahydrofuran / Ambient temperature

With hydrogenchloride; n-butyllithium; sulfuric acid; In tetrahydrofuran; ethanol; cyclohexane;

DOI:10.1021/jo00128a039

Reference yield:

1-bromo-octane (111-83-1) → 2-Nonanoylpyridine (143773-13-1)

Guidance literature:

Multi-step reaction with 2 steps

1: n-BuLi / tetrahydrofuran; cyclohexane / 1.) -78 deg C, 2.) 20 deg C, 30 min

2: aq. HCl / tetrahydrofuran / Ambient temperature

With hydrogenchloride; n-butyllithium; In tetrahydrofuran; cyclohexane;

DOI:10.1021/jo00128a039

upstream raw materials:

1-(1-Ethoxy-1-pyridin-2-yl-nonyl)-1H-benzotriazole

pyridine-2-carbaldehyde

1-bromo-octane

2-<(Benzotriazol-1-yl)ethoxymethyl>pyridine

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