6-Methoxypyridine-2-boronic acid MIDA ester

Base Information

Chemical Name:6-Methoxypyridine-2-boronic acid MIDA ester
CAS No.:1227700-45-9
Molecular Formula:C₁₁H₁₃BN₂O₅
Molecular Weight:264.046
Hs Code.:
Mol file:1227700-45-9.mol

Synonyms:6-methoxy-2-pyridylboronic acid N-methyliminodiacetic acid ester

Suppliers and Price of 6-Methoxypyridine-2-boronic acid MIDA ester

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

TRC
6-Methoxyl-2-pyridinylboronicAcidMIDAEster
500mg
$ 90.00

Sigma-Aldrich
6-Methoxy-2-pyridinylboronic acid MIDA ester
1g
$ 48.70

Sigma-Aldrich
6-Methoxy-2-pyridinylboronic acid MIDA ester
5g
$ 218.00

Crysdot
2-(6-Methoxypyridin-2-yl)-6-methyl-1,3,6,2-dioxazaborocane-4,8-dione 97%
5g
$ 220.00

American Custom Chemicals Corporation
6-METHOXYPYRIDINE-2-BORONIC ACID MIDA ESTER 95.00%
1G
$ 166.95

Alichem
2-(6-Methoxypyridin-2-yl)-6-methyl-1,3,6,2-dioxazaborocane-4,8-dione
1g
$ 400.00

Total 8 raw suppliers

Chemical Property of 6-Methoxypyridine-2-boronic acid MIDA ester

Chemical Property:

Melting Point:240-246°C
Storage Temp.:2-8°C

Purity/Quality:

98% ^*data from raw suppliers

6-Methoxyl-2-pyridinylboronicAcidMIDAEster ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Uses Reagent for coupling reactions 1 MIDA boronates as stable boronic acid surrogates for classically challenging cross-couplings. Suzuki Cross-Coupling with MIDA Boronates Reagent for coupling reactionsMIDA boronates as stable boronic acid surrogates for classically challenging cross-couplings.Suzuki Cross-Coupling with MIDA Boronates

Technology Process of 6-Methoxypyridine-2-boronic acid MIDA ester

There total 2 articles about 6-Methoxypyridine-2-boronic acid MIDA ester 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: 81.0%