Skip to Content
Merck
All Photos(3)

Key Documents

512346

Sigma-Aldrich

5-Formyl-2-furanylboronic acid

≥95%

Synonym(s):

5-Formyl-2-furanboronic acid

Sign Into View Organizational & Contract Pricing


About This Item

Empirical Formula (Hill Notation):
C5H5BO4
CAS Number:
Molecular Weight:
139.90
MDL number:
UNSPSC Code:
12352103
PubChem Substance ID:
NACRES:
NA.22

Quality Level

Assay

≥95%

form

solid

mp

136 °C (dec.) (lit.)

SMILES string

OB(O)c1ccc(C=O)o1

InChI

1S/C5H5BO4/c7-3-4-1-2-5(10-4)6(8)9/h1-3,8-9H

InChI key

JUWYQISLQJRRNT-UHFFFAOYSA-N

Application

Reactant involved in Suzuki coupling for synthesis of stable dye-senstitized solar cells

Reactant involved in synthesis of biologically active molecules including:
  • Heteroarylation for the synthesis of HIF-1 inhibitors
  • Disalicylic acid-furanyl derivatives to inhibit ephrin binding
  • HIV-1 integrase inhibitors
  • Epidermal growth factor receptor inhibitors

Other Notes

Contains varying amounts of anhydride

Pictograms

Corrosion

Signal Word

Danger

Hazard Statements

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’.

Already Own This Product?

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

Visit the Document Library

Qi Xia et al.
ACS applied materials & interfaces, 10(20), 17081-17088 (2018-05-03)
Effective long-term monitoring of tumor growth is significant for the evaluation of cancer therapy. Aggregation-induced emission-active near-infrared (NIR) fluorescent organic nanoparticles (TPFE-Rho dots) are designed and synthesized for long-term in vitro cell tracking and in vivo monitoring of tumor growth.
Marika Tiberi et al.
Antimicrobial agents and chemotherapy, 58(6), 3043-3052 (2014-03-13)
We report here the synthesis of 2-aminothiazolones along with their biological properties as novel anti-HIV agents. Such compounds have proven to act through the inhibition of the gp120-CD4 protein-protein interaction that occurs at the very early stage of the HIV-1

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