Skip to Content
Merck
CN

441651

3-Formylphenylboronic acid

≥95%

Synonym(s):

(3-Formylbenzene)boronic acid, 3-(Dihydroxyboryl)benzaldehyde, 3-Boronobenzaldehyde, m-Formylphenylboronic acid, m-formyl-benzeneboronic acid

Sign In to View Organizational & Contract Pricing.

Select a Size

About This Item

Linear Formula:
HCOC6H4B(OH)2
CAS Number:
87199-16-4
Molecular Weight:
149.94
UNSPSC Code:
12352103
NACRES:
NA.22
PubChem Substance ID:
24867694
MDL number:
MFCD00161356
Beilstein/REAXYS Number:
3030769

Key Documents

View All Documentation
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist

Product Name

3-Formylphenylboronic acid, ≥95%

InChI

1S/C7H7BO3/c9-5-6-2-1-3-7(4-6)8(10)11/h1-5,10-11H

SMILES string

OB(O)c1cccc(C=O)c1

InChI key

HJBGZJMKTOMQRR-UHFFFAOYSA-N

assay

≥95%

form

powder

mp

109-113 °C

functional group

aldehyde

Quality Level

100

Looking for similar products? Visit Product Comparison Guide

Related Categories

Application

Reagent used:
  • To study the effects of boronic acid on fluoride-selective chemosignaling behavior of merocyanine dye
  • As exciton-coupled CD probes for epigallocatechin gallate

Biological inhibitor of γ-glutamyltranspeptidase

Reactant involved in:
  • Palladium-catalyzed homocoupling
  • Suzuki coupling reactions

Other Notes

Contains varying amounts of anhydride

pictograms

Corrosion
GHS05

signalword

Danger

hcodes

H314

Hazard Classifications

Skin Corr. 1B

Storage Class

8A - Combustible corrosive hazardous materials

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
MKCW3833
SHBJ8153
SHBF3954V
80096PMV
80096PM

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

Mijun Peng et al.
Journal of chromatography. A, 1474, 8-13 (2016-11-09)
Rapid and efficient extraction of bioactive glycosides from complex natural origins poses a difficult challenge, and then is often inherent bottleneck for their highly utilization. Herein, we propose a strategy to fabricate boronate affinity based surface molecularly imprinted polymers (MIPs)
Hua-Wei Liu et al.
Chemistry, an Asian journal, 12(13), 1545-1556 (2017-04-19)
Sialic acids play important roles in mammalian development, cell-cell attachment, and signaling. As cancer cells utilize their overexpressed sialylated antigens to propagate metastases, the development of probes for sialic acids is of high importance. Herein, we report three luminescent cyclometalated

Related Content

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