1-Methylindole-2-boronic acid, pinacol ester

Base Information

Chemical Name:1-Methylindole-2-boronic acid, pinacol ester
CAS No.:596819-10-2
Molecular Formula:C15H20BNO2
Molecular Weight:257.14
Hs Code.:2933990090
Mol file:596819-10-2.mol

Synonyms:1-methylindole-2-boronic acid pinacol ester;1-METHYL-1H-INDOL-2-YLBORONIC ACID PINACOL ESTER;N-methyl-2-(4,4,5,5-tetramethyldioxaborolan-2-yl)indole;2-(4,4,5,5-tetramethyl-1,3,2,-dioxaborolan-2-yl)-N-methylindole;1-methyl-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indole;1-Methyl-2-indoleboronic acid pinacol ester;

Suppliers and Price of 1-Methylindole-2-boronic acid, pinacol 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

Sigma-Aldrich
1-Methyl-2-indoleboronic acid pinacol ester 97%
5g
$ 287.00

Sigma-Aldrich
1-Methyl-2-indoleboronic acid pinacol ester 97%
1g
$ 89.30

Crysdot
1-Methyl-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indole 95+%
5g
$ 337.00

Crysdot
1-Methyl-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indole 95+%
1g
$ 119.00

American Custom Chemicals Corporation
1-METHYL-2-INDOLEBORONIC ACID PINACOL ESTER 95.00%
1G
$ 189.00

AK Scientific
1-Methyl-2-indoleboronic acid pinacol ester
1g
$ 141.00

Total 11 raw suppliers

Chemical Property of 1-Methylindole-2-boronic acid, pinacol ester

Chemical Property:

Melting Point:97-101°C
PSA：23.39000
LogP:2.47750
Storage Temp.:?20°C

Purity/Quality:

97% ^*data from raw suppliers

1-Methyl-2-indoleboronic acid pinacol ester 97% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:Xi
Statements: 36/37/38
Safety Statements: 26

MSDS Files:: SDS file from LookChem

Useful:

Technology Process of 1-Methylindole-2-boronic acid, pinacol ester

There total 7 articles about 1-Methylindole-2-boronic acid, pinacol 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: 63.0%

: 46275-90-5
N-methyl-2-(1,1-dimethylethyl)indole

: 73183-34-3
bis(pinacol)diborane

: 596819-10-2
1-methyl-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indole

: 99810-76-1
2-(tert-butyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

Guidance literature:: N-methyl-2-(1,1-dimethylethyl)indole; bis(pinacol)diborane; With Trimethyl borate; triethylamine; In octane; at 160 ℃; for 48h;

With hydrogenchloride; In water; for 0.5h; regioselective reaction;
DOI:10.1039/d1sc04487g

Reference yield: 63.0%

: 133165-98-7
1-methyl-2-n-propyl-1H-indole

: 73183-34-3
bis(pinacol)diborane

: 596819-10-2
1-methyl-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indole

: 67562-19-0
4,4,5,5-tetramethyl-2-n-propyl-1,3,2-dioxaborolane

Guidance literature:: 1-methyl-2-n-propyl-1H-indole; bis(pinacol)diborane; With Trimethyl borate; triethylamine; In octane; at 160 ℃; for 48h;

With hydrogenchloride; In water; for 0.5h; regioselective reaction;
DOI:10.1039/d1sc04487g