3-(4-Bromophenoxy)propan-1-ol

Base Information

• Chemical Name: 3-(4-Bromophenoxy)propan-1-ol
• CAS No.: 67900-64-5
• Molecular Formula: C9H11BrO2
• Molecular Weight: 231.089
• European Community (EC) Number: 849-491-0
• DSSTox Substance ID: DTXSID00596034
• Wikidata: Q82491162
• Mol file: 67900-64-5.mol

Synonyms:3-(4-bromophenoxy)propan-1-ol;67900-64-5;1-Propanol, 3-(4-bromophenoxy)-;3-(4-bromophenoxy)-1-Propanol;SCHEMBL577534;3-(4-bromophenoxyl)propan-1-ol;DTXSID00596034;PFKPRUNICVIARC-UHFFFAOYSA-N;3-(4-Bromo-phenoxy)-propan-1-ol;MFCD11614020;AKOS005363328;AS-43014;DA-03693;EN300-77962;Z425795726

Chemical Property of 3-(4-Bromophenoxy)propan-1-ol

Chemical Property:

• XLogP3: 2.3
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 4
• Exact Mass: 229.99424
• Heavy Atom Count: 12
• Complexity: 111

Purity/Quality:

99% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1=CC(=CC=C1OCCCO)Br

Technology Process of 3-(4-Bromophenoxy)propan-1-ol

There total 9 articles about 3-(4-Bromophenoxy)propan-1-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: 100.0%

4-bromo-phenol (106-41-2) + 1-bromo-3-propanol (627-18-9) → 3-(4-Bromophenoxy)-1-propanol (67900-64-5)

Guidance literature:

With potassium carbonate; In N,N-dimethyl-formamide; at 20 ℃; for 12h;

Reference yield: 86.0%

potassium (3-(4-bromophenoxy)propyl)trifluoroborate → 3-(4-Bromophenoxy)-1-propanol (67900-64-5)

Guidance literature:

With rose bengal; triethylamine; In ethanol; at 25 ℃; for 12h; Schlenk technique; Irradiation;

DOI:10.1021/acs.orglett.8b02095

Reference yield: 81.0%

4-bromo-phenol (106-41-2) + 1-chloro-3-hydroxypropane (627-30-5) → 3-(4-Bromophenoxy)-1-propanol (67900-64-5)

Guidance literature:

With potassium carbonate; potassium iodide; In N,N-dimethyl-formamide; at 120 ℃; for 20h; Schlenk technique;

DOI:10.1016/j.tetlet.2015.08.061

upstream raw materials:

4-bromo-phenol

1-chloro-3-hydroxypropane

1-bromo-3-propanol

butanone

Downstream raw materials:

1-bromo-4-[3-(trityloxy)propoxy]benzene

3-(4-azidophenoxy)-propan-1-ol

4-[4-(3-hydroxypropoxy)phenyl]-2-methyl-3-butyn-2-ol

3-(4-ethynylphenoxy)propan-1-ol