3-Chlorophenyl boronic acid
3-Chlorophenylboronic acid is employed as a reactant involved in 1,4-conjugate addition reactions with ethenesulfonamides to form arylethanesulfonamides, Suzuki-Miyaura reactions with dibromotrifluoromethylbenzene, cross-coupling reactions with diazoesters3 or potassium cyanate. 3-Chlorophenylboronic acid is involved in the synthesis of biarylketones and phthalides and synthesis of inhibitors including PDE4 inhibitors among others. 3-Chlorophenyl boronic acid can affect cell migration. 3-Chlorophenyl boronic acid can be used to study wound healing [1].
Product Specifications
CAS Number
[63503-60-6]
UNSPSC
12352200
Hazard Statement
H302+H312+H332
Target
Biochemical Assay Reagents
Type
Biochemical Assay Reagents
Related Pathways
Others
Field of Research
Others
Assay Protocol
https://www.medchemexpress.com/3-chlorophenyl-boronic-acid.html
Purity
99.97
Solubility
DMSO : ≥ 200 mg/mL
Smiles
ClC1=CC=CC(B(O)O)=C1
Molecular Formula
C6H6BClO2
Molecular Weight
156.38
Precautions
H302+H312+H332
References & Citations
Shipping Conditions
Room Temperature
Storage Conditions
-20°C, 3 years; 4°C, 2 years (Powder)
Scientific Category
Biochemical Assay Reagents
Clinical Information
No Development Reported
Available Sizes
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