Skip to Content
Merck
CN

574686

3-Aminophenylboronic acid pinacol ester

97%

Synonym(s):

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

Sign In to View Organizational & Contract Pricing.

Select a Size

Change View

About This Item

Empirical Formula (Hill Notation):
C12H18BNO2
CAS Number:
Molecular Weight:
219.09
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352103
MDL number:
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist


Quality Level

assay

97%

mp

90-94 °C (lit.)

SMILES string

CC1(C)OB(OC1(C)C)c2cccc(N)c2

InChI

1S/C12H18BNO2/c1-11(2)12(3,4)16-13(15-11)9-6-5-7-10(14)8-9/h5-8H,14H2,1-4H3

InChI key

YMXIIVIQLHYKOT-UHFFFAOYSA-N

Application

3-Aminophenylboronic acid pinacol ester can be used:
  • As a starting material for the synthesis of 6-(hetero)arylthieno[3,2-b]pyridines, which are known to inhibit human tumor cells selectively.
  • In the functionalization of deuteroporphyrin IX dimethyl ester through Suzuki-Miyaura coupling.
  • To prepare benzo[d]oxazole based type-I FLT3-ITD inhibitors.

Legal Information

Product of Boron Molecular


pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

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

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk

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

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.

Already Own This Product?

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

Visit the Document Library



Functionalization of Deutero-and Protoporphyrin IX Dimethyl Esters via Palladium-Catalyzed Coupling Reactions
O?Brien JM, et al.
The Journal of Organic Chemistry, 84(10), 6158-6173 (2019)
Efficient synthesis of 6-(hetero) arylthieno [3, 2-b] pyridines by Suzuki-Miyaura coupling. Evaluation of growth inhibition on human tumor cell lines, SARs and effects on the cell cycle
Queiroz M-J, et al.
European Journal of Medicinal Chemistry, 45(12), 5628-5634 (2010)
Discovery of benzo [d] oxazole derivatives as the potent type-I FLT3-ITD inhibitors
Bao J, et al.
Bioorganic Chemistry, 94(10), 103248-103248 (2020)



Global Trade Item Number

SKUGTIN
574686-5G04061833356326
574686-1G04061832628073