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441651

Sigma-Aldrich

3-Formylphenylboronic acid

≥95%

Synonym(s):

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

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About This Item

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

Quality Level

100

Assay

≥95%

form

powder

mp

109-113 °C

SMILES string

OB(O)c1cccc(C=O)c1

InChI

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

InChI key

HJBGZJMKTOMQRR-UHFFFAOYSA-N

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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

Signal Word

Danger

Hazard Statements

H314

Precautionary Statements

P280 - P305 + P351 + P338 - P310

Hazard Classifications

Skin Corr. 1B

Storage Class Code

8A - Combustible corrosive hazardous materials

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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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

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