1-Chloro-3-(2-prop-2-enoxyphenoxy)propan-2-ol

Base Information

Chemical Name:1-Chloro-3-(2-prop-2-enoxyphenoxy)propan-2-ol
CAS No.:6452-74-0
Molecular Formula:C₁₂H₁₅ClO₃
Molecular Weight:242.702
Hs Code.:
DSSTox Substance ID:DTXSID701222854

Synonyms:6452-74-0;SCHEMBL11337572;DTXSID701222854;1-Chloro-3-[2-(2-propen-1-yloxy)phenoxy]-2-propanol

Suppliers and Price of 1-Chloro-3-(2-prop-2-enoxyphenoxy)propan-2-ol

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 1-Chloro-3-(2-prop-2-enoxyphenoxy)propan-2-ol

Chemical Property:

XLogP3:2.3
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:7
Exact Mass:242.0709720
Heavy Atom Count:16
Complexity:199

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C=CCOC1=CC=CC=C1OCC(CCl)O

Technology Process of 1-Chloro-3-(2-prop-2-enoxyphenoxy)propan-2-ol

There total 1 articles about 1-Chloro-3-(2-prop-2-enoxyphenoxy)propan-2-ol 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:

: 6452-74-0
3-(o-Allyloxyphenoxy)-2-hydroxy-1-chlorpropan

Guidance literature:: Epoxid II, HCl;

Reference yield:

: 6452-74-0
3-(o-Allyloxyphenoxy)-2-hydroxy-1-chlorpropan

: 75-31-0
isopropylamine

: 6452-71-7
oxprenolol

Guidance literature:: DOI:10.1021/jm00304a018

Reference yield:

: 6452-74-0
3-(o-Allyloxyphenoxy)-2-hydroxy-1-chlorpropan

: 6452-71-7,22972-96-9,22972-98-1,31576-00-8
(-)-Oxprenolol

Guidance literature:: Multi-step reaction with 3 steps

2: t-BuOK / tetrahydrofuran / 1 h / 0 °C

3: tetrahydrofuran; ethanol / 12 h / Heating

With potassium tert-butylate; In tetrahydrofuran; ethanol;
DOI:10.1016/S0957-4166(00)80256-6