13331-27-6
13331-27-6
Chemical Structure
3-Nitrophenylboronic acid
- CAS No.: 13331-27-6
- Formula:C6H6BNO4
- Molecular Weight:166.93
IUPAC Name: (3-nitrophenyl)boronic acid
InChIKey: ZNRGSYUVFVNSAW-UHFFFAOYSA-N
SMILES: OB(C1=CC=CC([N+]([O-])=O)=C1)O
Biological Activity: 3-Nitrophenylboronic acid is a biochemical reagent that can be used as a biological material or organic compound for life science related research.
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3-Nitrophenylboronic acid | 99.24% | 3-Nitrophenylboronic acid is a biochemical reagent that can be used as a biological material or organic compound for life science related research. | ||||||||||||||||||||
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3-Nitrophenylhydrazine-13C6 hydrochloride | 95.01% | 3-Nitrophenylhydrazine-13C6 (hydrochloride) is the 13C labeled 3-Nitrophenylhydrazine hydrochloride. | ||||||||||||||||||||
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4-Nitrophenylboronic acid | 99.66% | 4-Nitrophenylboronic acid is a biochemical reagent that can be used as a biological material or organic compound for life science related research. | ||||||||||||||||||||
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3-Aminophenylboronic acid monohydrate | 99.50% | 3-Aminophenylboronic acid monohydrate is a phenylboronic acid derivative. 3-Aminophenylboronic acid monohydrate reacts covalently with cis-diol groups of glycoproteins, enabling selective capture and detection of glycoproteins through fluorescence quenching of APBA-functionalized copper nanoclusters. | ||||||||||||||||||||
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3-Chlorophenyl boronic acid | 99.88% | 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 . | ||||||||||||||||||||
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3-Formylphenylboronic acid | 98.04% | 3-Formylphenylboronic acid is a biochemical reagent that can be used as a biological material or organic compound for life science related research. | ||||||||||||||||||||
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2-Nitrophenylboronic acid | 99.74% | 2-Nitrophenylboronic acid is a small-molecule arylboronic acid reagent selective for cysteine residues that mediates nickel (II)-promoted arylation of cysteine thiols. 2-Nitrophenylboronic acid is used in research related to peptide modification and also serves as a substrate for Suzuki-Miyaura coupling reactions in research related to organic synthesis. | ||||||||||||||||||||
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m-Fluoronitrobenzene | 99.64% | m-Fluoronitrobenzene (1-Fluoro-3-nitrobenzene) is a meta-substituted benzene derivative bearing fluoro and nitro functional groups. m-Fluoronitrobenzene finds applications in the fields of pharmaceuticals, dyes, pesticides, and synthetic rubber. | ||||||||||||||||||||
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3-Aminophenylboronic acid | 99.93% | 3-Aminophenylboronic acid (m-Aminophenylboronic acid) is a phenylboronic acid derivative. 3-Aminophenylboronic acid reacts covalently with cis-diol groups of glycoproteins, enabling selective capture and detection of glycoproteins through fluorescence quenching of APBA-functionalized copper nanoclusters. | ||||||||||||||||||||
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3-Nitrobenzaldoxime | 3-Nitrobenzaldoxime is a stain with biological research applications. | |||||||||||||||||||||
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3-Nitrobenzoic acid | 99.91% | 3-Nitrobenzoic acid (m-Carboxynitrobenzene; m-Nitrobenzenecarboxylic acid; m-Nitrobenzoic acid) is an antioxidant and antibacterial agent that can kill bacteria and fungi. 3-Nitrobenzoic acid can be degraded or reduced by certain bacteria (such as Pseudomonas) and fungi (such as white rot fungi) into aldehydes and alcohols. | ||||||||||||||||||||
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