3-Allyl-4-(allyloxy)-5-methoxybenzaldehyde

Base Information

Chemical Name:3-Allyl-4-(allyloxy)-5-methoxybenzaldehyde
CAS No.:861528-78-1
Molecular Formula:C14H16O3
Molecular Weight:232.279
Hs Code.:
DSSTox Substance ID:DTXSID90406355
Wikidata:Q82211282

Synonyms:3-ALLYL-4-(ALLYLOXY)-5-METHOXYBENZALDEHYDE;861528-78-1;3-methoxy-4-prop-2-enoxy-5-prop-2-enylbenzaldehyde;CHEMBRDG-BB 6437586;DTXSID90406355;MFCD02629579;AKOS000287203;BS-36083

Suppliers and Price of 3-Allyl-4-(allyloxy)-5-methoxybenzaldehyde

Supply Marketing:

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

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 5 raw suppliers

Chemical Property of 3-Allyl-4-(allyloxy)-5-methoxybenzaldehyde

Chemical Property:

Vapor Pressure:4.09E-05mmHg at 25°C
Boiling Point:351.5°C at 760 mmHg
Flash Point:157.6°C
Density:1.048g/cm³
XLogP3:3
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:7
Exact Mass:232.109944368
Heavy Atom Count:17
Complexity:262

Purity/Quality:: 98% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:COC1=CC(=CC(=C1OCC=C)CC=C)C=O

Technology Process of 3-Allyl-4-(allyloxy)-5-methoxybenzaldehyde

There total 3 articles about 3-Allyl-4-(allyloxy)-5-methoxybenzaldehyde 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:

: 20240-58-8
3-allyl-4-hydroxy-5-methoxybenzaldehyde

: 106-95-6
allyl bromide

: 861528-78-1
C₁₄H₁₆O₃

Guidance literature:: With potassium carbonate; In acetone; for 6h; Reflux;
DOI:10.1016/j.ejmech.2014.03.079

Reference yield:

: 121-33-5,8014-42-4
vanillin

: 861528-78-1
C₁₄H₁₆O₃

Guidance literature:: Multi-step reaction with 3 steps

1: potassium carbonate / acetone / 6 h / Reflux

2: 0.25 h / 195 - 205 °C / Microwave irradiation

3: potassium carbonate / acetone / 6 h / Reflux

With potassium carbonate; In acetone; 2: |Claisen Rearrangement;
DOI:10.1016/j.ejmech.2014.03.079

Reference yield:

: 22280-95-1
4-allyloxy-3-methoxybenzaldehyde

: 861528-78-1
C₁₄H₁₆O₃

Guidance literature:: Multi-step reaction with 2 steps

1: 0.25 h / 195 - 205 °C / Microwave irradiation

2: potassium carbonate / acetone / 6 h / Reflux

With potassium carbonate; In acetone; 1: |Claisen Rearrangement;
DOI:10.1016/j.ejmech.2014.03.079