Benzaldehyde, 3-[4-(bromomethyl)phenoxy]-4-methoxy-

Base Information

Chemical Name:Benzaldehyde, 3-[4-(bromomethyl)phenoxy]-4-methoxy-
CAS No.:111436-61-4
Molecular Formula:C15H13BrO3
Molecular Weight:321.17
Hs Code.:
DSSTox Substance ID:DTXSID70461043
Wikidata:Q82285271

Synonyms:111436-61-4;Benzaldehyde, 3-[4-(bromomethyl)phenoxy]-4-methoxy-;DTXSID70461043

Suppliers and Price of Benzaldehyde, 3-[4-(bromomethyl)phenoxy]-4-methoxy-

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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 Benzaldehyde, 3-[4-(bromomethyl)phenoxy]-4-methoxy-

Chemical Property:

XLogP3:3.4
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:5
Exact Mass:320.00481
Heavy Atom Count:19
Complexity:277

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:COC1=C(C=C(C=C1)C=O)OC2=CC=C(C=C2)CBr

Technology Process of Benzaldehyde, 3-[4-(bromomethyl)phenoxy]-4-methoxy-

There total 9 articles about Benzaldehyde, 3-[4-(bromomethyl)phenoxy]-4-methoxy- 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: 87.0%

: 208399-64-8
{4-[5-(1,3-dioxolan-2-yl)-2-methoxyphenoxy]phenyl}methanol

: 111436-61-4
3-[4-(bromomethyl)phenoxy]-4-methoxybenzaldehyde

Guidance literature:: With carbon tetrabromide; triphenylphosphine; In dichloromethane; at 0 - 20 ℃;
DOI:10.1002/anie.200500466

Reference yield:

: 621-59-0
isovanillin

: 111436-61-4
3-[4-(bromomethyl)phenoxy]-4-methoxybenzaldehyde

Guidance literature:: Multi-step reaction with 4 steps

1: 84 percent / pyridinium p-toluenesulfonate / benzene / Heating

2: 90 percent / potassium carbonate / dimethylformamide / 19 h / 155 °C

3: 92 percent / sodium borohydride / methanol / 1 h / 0 °C

4: 87 percent / triphenylphosphine; carbon tetrabromide / CH₂Cl₂ / 0 - 20 °C

With sodium tetrahydroborate; carbon tetrabromide; pyridinium p-toluenesulfonate; potassium carbonate; triphenylphosphine; In methanol; dichloromethane; N,N-dimethyl-formamide; benzene;
DOI:10.1002/anie.200500466