4-Penten-2-ol, 1-(4-methoxyphenoxy)-, (2R)-

Base Information

Chemical Name:4-Penten-2-ol, 1-(4-methoxyphenoxy)-, (2R)-
CAS No.:351026-61-4
Molecular Formula:C12H16O3
Molecular Weight:208.257
Hs Code.:
DSSTox Substance ID:DTXSID30460491
Nikkaji Number:J1.530.970I
Wikidata:Q82284548
Mol file:351026-61-4.mol

Synonyms:4-Penten-2-ol, 1-(4-methoxyphenoxy)-, (2R)-;351026-61-4;DTXSID30460491

Suppliers and Price of 4-Penten-2-ol, 1-(4-methoxyphenoxy)-, (2R)-

Supply Marketing:

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

Manufacturers and distributors:

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Chemical Property of 4-Penten-2-ol, 1-(4-methoxyphenoxy)-, (2R)-

Chemical Property:

XLogP3:2.4
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:6
Exact Mass:208.109944368
Heavy Atom Count:15
Complexity:174

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:COC1=CC=C(C=C1)OCC(CC=C)O
Isomeric SMILES:COC1=CC=C(C=C1)OC[C@@H](CC=C)O

Technology Process of 4-Penten-2-ol, 1-(4-methoxyphenoxy)-, (2R)-

There total 2 articles about 4-Penten-2-ol, 1-(4-methoxyphenoxy)-, (2R)- 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: 95.0%

: 3536-96-7
vinylmagnesium chloride

: 2211-94-1,51469-79-5,71048-65-2,71031-04-4,26744-15-0
4-methoxybenzyloxy ester of (S)-glycidol

: 351026-61-4
(R)-1-(4-Methoxy-phenoxy)-pent-4-en-2-ol

Guidance literature:: With copper(l) iodide; In tetrahydrofuran; at -40 ℃;
DOI:10.1021/ol016116x

Reference yield:

: 150-76-5
4-methoxy-phenol

: 351026-61-4
(R)-1-(4-Methoxy-phenoxy)-pent-4-en-2-ol

Guidance literature:: Multi-step reaction with 2 steps

1: 82 percent / Ph₃P; DEAD / tetrahydrofuran / 15 h / 0 °C

2: 95 percent / CuI / tetrahydrofuran / -40 °C

With copper(l) iodide; triphenylphosphine; diethylazodicarboxylate; In tetrahydrofuran; 1: Mitsunobu reaction;
DOI:10.1021/ol016116x