2,6-Dimethoxy-4-propylbenzeneacetaldehyde

Base Information

Chemical Name:2,6-Dimethoxy-4-propylbenzeneacetaldehyde
CAS No.:203912-56-5
Molecular Formula:C₁₃H₁₈O₃
Molecular Weight:222.284
Hs Code.:
DSSTox Substance ID:DTXSID401270311

Synonyms:SCHEMBL8704103;DTXSID401270311;2,6-Dimethoxy-4-propylbenzeneacetaldehyde;203912-56-5

Suppliers and Price of 2,6-Dimethoxy-4-propylbenzeneacetaldehyde

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of 2,6-Dimethoxy-4-propylbenzeneacetaldehyde

Chemical Property:

XLogP3:2.6
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:6
Exact Mass:222.125594432
Heavy Atom Count:16
Complexity:191

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CCCC1=CC(=C(C(=C1)OC)CC=O)OC

Technology Process of 2,6-Dimethoxy-4-propylbenzeneacetaldehyde

There total 3 articles about 2,6-Dimethoxy-4-propylbenzeneacetaldehyde 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: 20.0%

: 41395-10-2
1,3-dimethoxy-5-propylbenzene

: 2032-35-1
Bromoacetaldehyde diethyl acetal

: 203912-56-5
2,6-dimethoxy-4-n-propylphenylacetaldehyde

Guidance literature:: 1,3-dimethoxy-5-propylbenzene; With n-butyllithium; In hexane; cyclohexane; for 1.5h; Heating;

Bromoacetaldehyde diethyl acetal; In hexane; cyclohexane; for 1.5h; Heating;

With hydrogenchloride; In ethanol; at 20 ℃;
DOI:10.1002/1521-4184(200102)334:2<53::AID-ARDP53>3.0.CO;2-C

Reference yield:

: 7311-34-4
3,5-dimethoxybenzaldehdye

: 203912-56-5
2,6-dimethoxy-4-n-propylphenylacetaldehyde

Guidance literature:: Multi-step reaction with 3 steps

1.1: Mg / diethyl ether

1.2: 88 percent / diethyl ether / 2 h / Heating

2.1: 68 percent / H₂ / 10 percent Pd/C / acetic acid / 30 h / 20 °C

3.1: nBuLi / cyclohexane; hexane / 1.5 h / Heating

3.2: cyclohexane; hexane / 1.5 h / Heating

3.3: 20 percent / HCl / ethanol / 20 °C

With n-butyllithium; hydrogen; magnesium; palladium on activated charcoal; In diethyl ether; hexane; cyclohexane; acetic acid; 1.2: Grignard reaction;
DOI:10.1002/1521-4184(200102)334:2<53::AID-ARDP53>3.0.CO;2-C

Reference yield:

: 203912-55-4
1-(3,5-dimethoxy-phenyl)-propan-1-ol

: 203912-56-5
2,6-dimethoxy-4-n-propylphenylacetaldehyde

Guidance literature:: Multi-step reaction with 2 steps

1.1: 68 percent / H₂ / 10 percent Pd/C / acetic acid / 30 h / 20 °C

2.1: nBuLi / cyclohexane; hexane / 1.5 h / Heating

2.2: cyclohexane; hexane / 1.5 h / Heating

2.3: 20 percent / HCl / ethanol / 20 °C

With n-butyllithium; hydrogen; palladium on activated charcoal; In hexane; cyclohexane; acetic acid;
DOI:10.1002/1521-4184(200102)334:2<53::AID-ARDP53>3.0.CO;2-C