Methoxyethylbenzeneboronic acid, (S)-

Base Information

Chemical Name:Methoxyethylbenzeneboronic acid, (S)-
CAS No.:166191-23-7
Molecular Formula:C₉H₁₃BO₃
Molecular Weight:180.011
Hs Code.:
UNII:C0V9Y2OEUC
Wikidata:Q27275027

Synonyms:UNII-C0V9Y2OEUC;C0V9Y2OEUC;Methoxyethylbenzeneboronic acid, (S)-;Methoxyethylbenzeneboronic acid, (-)-;B-(2-((1S)-1-Methoxyethyl)phenyl)boronic acid;Methoxyethylbenzeneboronic acid (-)-S-form [MI];Boronic acid, B-(2-((1S)-1-methoxyethyl)phenyl)-;166191-23-7;(S)-methoxyethylbenzeneboronic acid;Q27275027

Suppliers and Price of Methoxyethylbenzeneboronic acid, (S)-

Supply Marketing:

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

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Chemical Property of Methoxyethylbenzeneboronic acid, (S)-

Chemical Property:

Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:3
Exact Mass:180.0957744
Heavy Atom Count:13
Complexity:152

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:B(C1=CC=CC=C1C(C)OC)(O)O
Isomeric SMILES:B(C1=CC=CC=C1[C@H](C)OC)(O)O

Technology Process of Methoxyethylbenzeneboronic acid, (S)-

There total 1 articles about Methoxyethylbenzeneboronic acid, (S)- 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: 50.0%

: 5419-55-6
Triisopropyl borate

: 166191-24-8
(S)-1-bromo-2-(1-methoxyethyl)benzene

: 166191-23-7
(-)-(S)-2-(1-methoxyethyl)benzeneboronic acid

Guidance literature:: With hydrogenchloride; water; tert.-butyl lithium; In diethyl ether; pentane; reaction of ether in Et2O with t-BuLi in pentane at -78°C, warmed to room temp., cooled to -78°C, addn. to B-compd. in Et2O at -78°C, stirred for 3 h (warmed to 25°C), addn. of HCl in Et2O, stirred for 1 h, hydrolized in H2O; recrystn. (n-hexane);