Boronic acid, [4-(dodecyloxy)phenyl]-

Base Information

Chemical Name:Boronic acid, [4-(dodecyloxy)phenyl]-
CAS No.:169760-27-4
Molecular Formula:C18H31BO3
Molecular Weight:306.253
Hs Code.:
Mol file:169760-27-4.mol

Synonyms:

Suppliers and Price of Boronic acid, [4-(dodecyloxy)phenyl]-

Supply Marketing:

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

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 12 raw suppliers

Chemical Property of Boronic acid, [4-(dodecyloxy)phenyl]-

Chemical Property:

Purity/Quality:: 99% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Technology Process of Boronic acid, [4-(dodecyloxy)phenyl]-

There total 7 articles about Boronic acid, [4-(dodecyloxy)phenyl]- 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%

: 123883-51-2
1-bromo-4-dodecyloxybenzene

: 169760-27-4
4-dodecyloxybenzene boronic acid

Guidance literature:: 1-bromo-4-dodecyloxybenzene; With n-butyllithium; Trimethyl borate;

With hydrogenchloride;
DOI:10.1080/10587250108025293

Reference yield: 65.7%

: 121-43-7,63156-11-6
Trimethyl borate

: 123883-51-2
1-bromo-4-dodecyloxybenzene

: 169760-27-4
4-dodecyloxybenzene boronic acid

Guidance literature:: 1-bromo-4-dodecyloxybenzene; With n-butyllithium; In tetrahydrofuran; diethyl ether; at -65 ℃; for 1h; Inert atmosphere;

Trimethyl borate; at -65 ℃; for 1h;
DOI:10.1021/acs.biomac.5b01325

Reference yield:

: 143-15-7
1-dodecylbromide

: 169760-27-4
4-dodecyloxybenzene boronic acid

Guidance literature:: Multi-step reaction with 2 steps

1.1: 100 percent / K₂CO₃

2.1: trimethyl borate; n-butyllithium

2.2: 100 percent / aq. HCl

With n-butyllithium; Trimethyl borate; potassium carbonate; 1.1: Williamson's etherification;
DOI:10.1080/10587250108025293