59016-93-2
59016-93-2
Chemical Structure
4-(Hydroxymethyl)benzeneboronic acid
- CAS No.: 59016-93-2
- Formula:C7H9BO3
- Molecular Weight:151.96
IUPAC Name: (4-(hydroxymethyl)phenyl)boronic acid
InChIKey: PZRPBPMLSSNFOM-UHFFFAOYSA-N
SMILES: OCC1=CC=C(B(O)O)C=C1
Biological Activity: 4-(Hydroxymethyl)benzeneboronic acid is an important intermediate. 4-(Hydroxymethyl)benzeneboronic acid can be used for the synthesis of other active compounds[1].
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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-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-Cyanobenzeneboronic acid | 99.99% | 4-Cyanobenzeneboronic acid is a boronic acid derivative and also coupling reagent in Suzuki cross-coupling reactions. | ||||||||||||||||||||
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4-Boronobenzoic acid | 99.81% | 4-Boronobenzoic acid is an organic compound. 4-Boronobenzoic acid forms reversible cyclic boronate esters with molecules containing cis-vicinal diol structures (such as sialic acid) through the boron atom, achieving molecular recognition and binding. 4-Boronobenzoic acid can be used in research of breast cancer . | ||||||||||||||||||||
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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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1,4-Phenylenediboronic acid | 99.38% | 1,4-Phenylenediboronic 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-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-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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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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