Skip to Content
MilliporeSigma
All Photos(1)

Key Documents

View All Documentation

578835

Sigma-Aldrich

5-Indoleboronic acid pinacol ester

97%

Synonym(s):

5-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indole

Sign Into View Organizational & Contract Pricing
All Photos(1)

About This Item

Empirical Formula (Hill Notation):
C14H18BNO2
CAS Number:
269410-24-4
Molecular Weight:
243.11
MDL number:
MFCD03789263
UNSPSC Code:
12352103
PubChem Substance ID:
24880953
NACRES:
NA.22

Quality Level

100

assay

97%

form

solid

mp

120-125 °C (lit.)

SMILES string

CC1(C)OB(OC1(C)C)c2ccc3[nH]ccc3c2

InChI

1S/C14H18BNO2/c1-13(2)14(3,4)18-15(17-13)11-5-6-12-10(9-11)7-8-16-12/h5-9,16H,1-4H3

InChI key

FATPQDPUKVVCLT-UHFFFAOYSA-N

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
MKCT4804
MKBL2603V
MKBJ0562V
MKBF2073V
MKBB9447

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Articles

Suzuki-Miyaura Cross-Coupling Reagents

Suzuki-Miyaura cross-coupling reaction is extensively used in organic chemistry, polymer science, and pharmaceutical industries.

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

Contact Technical Service