134150-01-9
134150-01-9
Chemical Structure
4-Propylphenylboronic acid
- CAS No.: 134150-01-9
- Formula:C9H13BO2
- Molecular Weight:164.01
IUPAC Name: (4-Propylphenyl)boronic acid
InChIKey: WLCGYIWOKVWFLB-UHFFFAOYSA-N
SMILES: C1=C(C=CC(=C1)CCC)B(O)O
Biological Activity: 4-Propylphenylboronic acid is a biochemical reagent that can be used as a biological material or organic compound for life science related research.
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
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4-Propylphenylboronic acid | 4-Propylphenylboronic 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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4-Tolylboronic acid | 99.77% | 4-Tolylboronic acid is an organoboron compound with important chemical applications. It can be used as an important intermediate in organic synthesis for the synthesis of organic compounds such as drugs, pesticides, and cosmetics, as well as for the research of coordination chemistry and material science. Due to its high chemical reactivity, 4-Tolylboronic acid has become a widely used reagent in organic synthesis. | ||||||||||||||||||||
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4-Acetylphenylboronic acid | 99.67% | 4-Acetylphenylboronic acid is a potent inhibitor of carbonic anhydrases II(CA II), with IC50s of 246 μM and 281.40 μM for bovine CA II (bCA II) and human CA II (hCA II). 4-Acetylphenylboronic acid can be obtained via mechanochemistry and solvent evaporation. 4-Acetylphenylboronic acid has a loss of the carbonyl group at 500-550 K. | ||||||||||||||||||||
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4-Fluorobenzeneboronic acid | 99.88% | 4-Fluorobenzeneboronic acid (P-Fluorophenylboronic acid) is a fluorinated arylboronic acid coupling ligand and precursor. Under the catalysis of heterogeneous palladium nanoparticles, 4-Fluorobenzeneboronic acid participates in the Suzuki-Miyaura C-C coupling reaction to generate fluorinated biphenyl derivatives. 4-Fluorobenzeneboronic acid also participates in the copper-catalyzed three-component reaction with nitrobenzene and potassium metabisulfite as substrates, and finally produces sulfonamides through the formation of arylsulfinate intermediates, copper-assisted S-N bond construction and reduction steps. | ||||||||||||||||||||
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4-(Hydroxymethyl)benzeneboronic acid | 99.94% | 4-(Hydroxymethyl)benzeneboronic acid is an important intermediate. 4-(Hydroxymethyl)benzeneboronic acid can be used for the synthesis of other active compounds. | ||||||||||||||||||||
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4-Methoxyphenylboronic acid | 99.83% | 4-Methoxyphenylboronic 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-Hydroxymethyl)phenylboronic acid | 98.27% | 3-(Hydroxymethyl)phenylboronic 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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4-Propylphenol | 99.80% | 4-Propylphenol is a plant-derived phenolic compound. 4-Propylphenol causes an increase in ROS within the Fusarium graminearum cells, leading to damage to the DNA and cell membranes of the mycelia, effectively inhibiting the growth of the mycelia. 4-Propylphenol also has a growth inhibitory effect on walnut pathogenic fungi (C. gloeosporioides, C. siamense, A. alternata), with its EC50 ranging from 29.11 to 31.89 mg/L, and it also inhibits spore germination, with EC50 being 55.04-71.85 mg/L. 4-Propylphenol can be used in the research of fungal diseases in walnuts and wheat Fusarium head blight. | ||||||||||||||||||||
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2-(4-Boronophenyl)acetic acid | 2-(4-Boronophenyl)acetic acid is a PROTAC linker that can be used in the synthesis of PROTACs. | |||||||||||||||||||||
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3-(4-Boronophenyl)propanoic acid | 3-(4-Boronophenyl)propanoic acid is a PROTAC linker that can be used in the synthesis of PROTACs. | |||||||||||||||||||||
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(4-(3-Methoxy-3-oxopropyl)phenyl)boronic acid | (4-(3-Methoxy-3-oxopropyl)phenyl)boronic acid is a PROTAC linker that can be used in the synthesis of PROTACs. | |||||||||||||||||||||
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