4,4'-Oxybis[2-(prop-2-en-1-yl)phenol]

Base Information

Chemical Name:4,4'-Oxybis[2-(prop-2-en-1-yl)phenol]
CAS No.:105329-34-8
Molecular Formula:C₁₈H₁₈O₃
Molecular Weight:282.339
Hs Code.:
DSSTox Substance ID:DTXSID30516705
Wikidata:Q82378242
Mol file:105329-34-8.mol

Synonyms:105329-34-8;4,4'-Oxybis[2-(prop-2-en-1-yl)phenol];SCHEMBL1951863;DTXSID30516705

Suppliers and Price of 4,4'-Oxybis[2-(prop-2-en-1-yl)phenol]

Supply Marketing:

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

Manufacturers and distributors:

Manufacture/Brand
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Total 0 raw suppliers

Chemical Property of 4,4'-Oxybis[2-(prop-2-en-1-yl)phenol]

Chemical Property:

XLogP3:4.8
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:6
Exact Mass:282.125594432
Heavy Atom Count:21
Complexity:309

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C=CCC1=C(C=CC(=C1)OC2=CC(=C(C=C2)O)CC=C)O

Technology Process of 4,4'-Oxybis[2-(prop-2-en-1-yl)phenol]

There total 4 articles about 4,4'-Oxybis[2-(prop-2-en-1-yl)phenol] 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:

: 1965-09-9
4,4'-dihydroxydiphenyl ether

: 105329-34-8
Bis-(4-hydroxy-3-allyl-phenyl)-aether

Guidance literature:: Multi-step reaction with 2 steps

1: K₂CO₃; acetone

2: 250 °C / 20 Torr

With potassium carbonate; acetone;
DOI:10.1021/ja01214a008

Reference yield:

: 101-80-4,121509-79-3
4,4'-oxydiphenylene diamine

: 105329-34-8
Bis-(4-hydroxy-3-allyl-phenyl)-aether

Guidance literature:: Multi-step reaction with 3 steps

1: Diazotization

2: K₂CO₃; acetone

3: 250 °C / 20 Torr

With potassium carbonate; acetone;
DOI:10.1021/ja01214a008