2,4-Dipropoxybenzaldehyde

Base Information

• Chemical Name: 2,4-Dipropoxybenzaldehyde
• CAS No.: 156744-09-1
• Molecular Formula: C13H18O3
• Molecular Weight: 222.284
• DSSTox Substance ID: DTXSID90368484
• Wikidata: Q82155051
• Mol file: 156744-09-1.mol

Synonyms:2,4-dipropoxybenzaldehyde;156744-09-1;2,4-Dipropoxy-benzaldehyde;Benzaldehyde, 2,4-dipropoxy-;SCHEMBL5449064;DTXSID90368484;AKOS000115386;CS-0218457;EN300-01036;Z53835424

Chemical Property of 2,4-Dipropoxybenzaldehyde

Chemical Property:

• PSA: 35.53000
• LogP: 3.07670
• XLogP3: 3.1
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 7
• Exact Mass: 222.125594432
• Heavy Atom Count: 16
• Complexity: 194

Purity/Quality:

99% ^*data from raw suppliers

2,4-dipropoxybenzaldehyde ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CCCOC1=CC(=C(C=C1)C=O)OCCC

Technology Process of 2,4-Dipropoxybenzaldehyde

There total 1 articles about 2,4-Dipropoxybenzaldehyde 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: 90.0%

propyl bromide (106-94-5) + 2,4-Dihydroxybenzaldehyde (95-01-2) → 2,4-dipropoxybenzaldehyde (156744-09-1)

Guidance literature:

With potassium carbonate; In N,N-dimethyl-formamide; at 85 ℃; for 3.5h;

DOI:10.1016/j.ejmech.2014.05.027

Reference yield: 89.8%

2,4-imidazolidinedione (461-72-3) + 2,4-dipropoxybenzaldehyde (156744-09-1) → (Z)-5-(2,4-dipropoxybenzylidene)imidazolidine-2,4-dione (1256244-51-5)

Guidance literature:

With sodium hydrogencarbonate; ethanolamine; In ethanol; water; pH=7; stereoselective reaction; Reflux;

DOI:10.1016/j.ejmech.2010.08.066

Reference yield: 86.0%

2-oxoindole (59-48-3) + 2,4-dipropoxybenzaldehyde (156744-09-1) → 3-(2,4-dipropoxybenzylidene)-1,3-dihydroindol-2-one

Guidance literature:

With piperidine; In ethanol; for 1.5h; Reflux;

DOI:10.1016/j.ejmech.2014.05.027

upstream raw materials:

propyl bromide

2,4-Dihydroxybenzaldehyde

Downstream raw materials:

(Z)-5-(2,4-dipropoxybenzylidene)imidazolidine-2,4-dione