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About This Item
Empirical Formula (Hill Notation):
C3H5BN2O2 · xH2O
Molecular Weight:
111.90 (anhydrous basis)
MDL number:
UNSPSC Code:
12352103
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
form
solid
mp
88-93 °C
storage temp.
2-8°C
SMILES string
O.OB(O)c1cc[nH]n1
InChI
1S/C3H5BN2O2.H2O/c7-4(8)3-1-2-5-6-3;/h1-2,7-8H,(H,5,6);1H2
InChI key
NXQCQMBEFQLICU-UHFFFAOYSA-N
General description
1H-Pyrazol-3-ylboronic acid hydrate can be used as a reactant in the Suzuki-Miyaura coupling reaction to synthesize pyrazole derivatives by reacting with different aryl halides over the palladium catalyst.[1]
Application
Reactant for:
- Preparation of receiver-amplifier, self-immolative dendrimers as potential platform for self-triggered multiple-release prodrugs
- Preparation of bifunctional water-soluble triazole-containing derivatives of ethyl(hydroxycamptothecin) via click chemistry and conjugation to monoclonal antibodies for anticancer therapy
- Intermediate for synthesis of oligo(ethylene glycol)-terminated alkanethiol amides useful for biosensors
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Target Organs
Respiratory system
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
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Novel Chemical Series of 5-Lipoxygenase-Activating Protein Inhibitors for Treatment of Coronary Artery Disease
Lemurell M, et al.
Journal of medicinal chemistry, 62(9), 4325-4349 (2019)
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