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640395

Sigma-Aldrich

1-Methylindole-5-boronic acid pinacol ester

97%

Synonym(s):

1-Methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indole, 1-Methyl-5-indoleboronic acid pinacol ester

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About This Item

Empirical Formula (Hill Notation):
C15H20BNO2
CAS Number:
Molecular Weight:
257.14
MDL number:
UNSPSC Code:
12352103
PubChem Substance ID:
NACRES:
NA.22

Quality Level

assay

97%

form

solid

mp

110-114 °C (lit.)

SMILES string

Cn1ccc2cc(ccc12)B3OC(C)(C)C(C)(C)O3

InChI

1S/C15H20BNO2/c1-14(2)15(3,4)19-16(18-14)12-6-7-13-11(10-12)8-9-17(13)5/h6-10H,1-5H3

InChI key

JQLYKUPEQYNDFF-UHFFFAOYSA-N

Related Categories

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)


Certificates of Analysis (COA)

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Articles

This brochure contains a comprehensive selection of boronic acids, boronic acid esters, diboron esters, and transition-metal catalysts useful for the Suzuki–Miyaura coupling reaction

The synthesis of biaryl compounds via the Suzuki–Miyaura coupling reaction has become more commonplace now that many arylboronic acids are readily available.

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

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