2-(2-(4-Bromophenyl)-5-methyloxazol-4-YL)ethanol

Base Information

Chemical Name:2-(2-(4-Bromophenyl)-5-methyloxazol-4-YL)ethanol
CAS No.:328918-84-9
Molecular Formula:C₁₂H₁₂BrNO₂
Molecular Weight:282.137
Hs Code.:
DSSTox Substance ID:DTXSID701262610

Synonyms:328918-84-9;2-(2-(4-BROMOPHENYL)-5-METHYLOXAZOL-4-YL)ETHANOL;2-(4-Bromophenyl)-5-methyl-4-oxazoleethanol;SCHEMBL1981068;SBNVFWXTMCXMBN-UHFFFAOYSA-N;DTXSID701262610;2-[2-(4-bromo-phenyl)-5-methyl-oxazol-4-yl]-ethanol

Suppliers and Price of 2-(2-(4-Bromophenyl)-5-methyloxazol-4-YL)ethanol

Supply Marketing:

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

Manufacturers and distributors:

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Chemicals and raw materials
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Total 1 raw suppliers

Chemical Property of 2-(2-(4-Bromophenyl)-5-methyloxazol-4-YL)ethanol

Chemical Property:

XLogP3:2.7
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:3
Exact Mass:281.00514
Heavy Atom Count:16
Complexity:219

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CC1=C(N=C(O1)C2=CC=C(C=C2)Br)CCO

Technology Process of 2-(2-(4-Bromophenyl)-5-methyloxazol-4-YL)ethanol

There total 7 articles about 2-(2-(4-Bromophenyl)-5-methyloxazol-4-YL)ethanol 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: 72.0%

: 328918-82-7
2-(4-bromophenyl)-5-methyl-4-oxazoleacetic acid

: 328918-84-9
2-(4-bromophenyl)-5-methyl-4-oxazoleethanol

Guidance literature:: With borane; In tetrahydrofuran; methanol;
DOI:10.1016/j.bmcl.2004.09.031

Reference yield:

: 328918-81-6
2-(4-bromophenyl)-4-(chloromethyl)-5-methyl-1,3-oxazole

: 328918-84-9
2-(4-bromophenyl)-5-methyl-4-oxazoleethanol

Guidance literature:: Multi-step reaction with 3 steps

1: 100 percent / KI / dimethylformamide

2: 60 percent / KOH / 2-methoxy-ethanol

3: 72 percent / BH₃ / tetrahydrofuran; methanol

With potassium hydroxide; borane; potassium iodide; In tetrahydrofuran; methanol; 2-methoxy-ethanol; N,N-dimethyl-formamide;
DOI:10.1016/j.bmcl.2004.09.031

Reference yield:

: 328918-83-8
[2-(4-bromophenyl)-5-methyloxazole-4-yl]-acetonitrile

: 328918-84-9
2-(4-bromophenyl)-5-methyl-4-oxazoleethanol

Guidance literature:: Multi-step reaction with 2 steps

1: 60 percent / KOH / 2-methoxy-ethanol

2: 72 percent / BH₃ / tetrahydrofuran; methanol

With potassium hydroxide; borane; In tetrahydrofuran; methanol; 2-methoxy-ethanol;
DOI:10.1016/j.bmcl.2004.09.031