3-[4-(Hexyloxy)phenyl]prop-2-enal

Base Information

Chemical Name:3-[4-(Hexyloxy)phenyl]prop-2-enal
CAS No.:149365-08-2
Molecular Formula:C15H20O2
Molecular Weight:232.323
Hs Code.:
DSSTox Substance ID:DTXSID70705590
Mol file:149365-08-2.mol

Synonyms:149365-08-2;3-[4-(Hexyloxy)phenyl]prop-2-enal;DTXSID70705590

Suppliers and Price of 3-[4-(Hexyloxy)phenyl]prop-2-enal

Supply Marketing:

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

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Chemical Property of 3-[4-(Hexyloxy)phenyl]prop-2-enal

Chemical Property:

XLogP3:4.1
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:8
Exact Mass:232.146329876
Heavy Atom Count:17
Complexity:215

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCCCCCOC1=CC=C(C=C1)C=CC=O

Technology Process of 3-[4-(Hexyloxy)phenyl]prop-2-enal

There total 5 articles about 3-[4-(Hexyloxy)phenyl]prop-2-enal 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: 71.0%

: 107771-21-1
1-hexyloxy-4-vinylbenzene

: 68-12-2,33513-42-7
N,N-dimethyl-formamide

: 149365-08-2
3-(4-hexyloxyphenyl)propenal

Guidance literature:: With trichlorophosphate; at 60 - 70 ℃; for 0.333333h;

Reference yield: 50.0%

: 2-[(E)-2-(4-Hexyloxy-phenyl)-vinyl]-[1,3]dioxolane

: 149365-08-2
3-(4-hexyloxyphenyl)propenal

Guidance literature:: With hydrogenchloride; In tetrahydrofuran; for 3h;

Reference yield:

: 5736-94-7
4-(hexyloxy)benzaldehyde

: 149365-08-2
3-(4-hexyloxyphenyl)propenal

Guidance literature:: Multi-step reaction with 2 steps

1: LiOCH₃ / methanol; dimethylformamide / 8 h / Heating

2: 50 percent / 10percent aq. HCl / tetrahydrofuran / 3 h

With hydrogenchloride; lithium methanolate; In tetrahydrofuran; methanol; N,N-dimethyl-formamide;