3-Pentyn-2-ol, 5-(4-fluorophenoxy)-

Base Information

Chemical Name:3-Pentyn-2-ol, 5-(4-fluorophenoxy)-
CAS No.:305805-77-0
Molecular Formula:C11H11FO2
Molecular Weight:194.206
Hs Code.:
DSSTox Substance ID:DTXSID00461910
Nikkaji Number:J1.376.996F
Mol file:305805-77-0.mol

Synonyms:3-Pentyn-2-ol, 5-(4-fluorophenoxy)-;305805-77-0;DTXSID00461910

Suppliers and Price of 3-Pentyn-2-ol, 5-(4-fluorophenoxy)-

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 3-Pentyn-2-ol, 5-(4-fluorophenoxy)-

Chemical Property:

XLogP3:1.8
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:2
Exact Mass:194.07430775
Heavy Atom Count:14
Complexity:220

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CC(C#CCOC1=CC=C(C=C1)F)O

Technology Process of 3-Pentyn-2-ol, 5-(4-fluorophenoxy)-

There total 2 articles about 3-Pentyn-2-ol, 5-(4-fluorophenoxy)- 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: 84.0%

: 75-07-0,9002-91-9
acetaldehyde

: 124700-26-1
1-fluoro-4-(2-propynyloxy)benzene

: 305805-77-0
5-(4-fluorophenoxy)pent-3-yn-2-ol

Guidance literature:: 1-fluoro-4-(2-propynyloxy)benzene; With ethylmagnesium bromide; In tetrahydrofuran; at 0 ℃;

acetaldehyde; In tetrahydrofuran; at 0 ℃;
DOI:10.3987/COM-00-8964

Reference yield:

: 371-41-5
4-Fluorophenol

: 305805-77-0
5-(4-fluorophenoxy)pent-3-yn-2-ol

Guidance literature:: Multi-step reaction with 2 steps

1.1: 87 percent / potassium carbonate / acetone / 18 h / 50 °C

2.1: ethylmagnesium bromide / tetrahydrofuran / 0 °C

2.2: 84 percent / tetrahydrofuran / 0 °C

With ethylmagnesium bromide; potassium carbonate; In tetrahydrofuran; acetone; 1.1: Etherification / 2.1: Metallation / 2.2: Grignard reaction;
DOI:10.3987/COM-00-8964