Boronic acid derivatives

Organic compounds that are derived from boronic acid; boronic acid is an oxyacid of boron with the following structure: H2BOH.

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916 – 930 of 2,761 results

916

Aobchem AOBCHEM

5000952275 2-CHLORO-5-ETHOXYPHENYLBORONIC

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917

Aobchem AOBCHEM

5001056736 2-FLUOROPHENYLBORONIC ACID 100

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918

Aobchem AOBCHEM

5001056772 4-CYANOPHENYLBORONIC ACID 100G

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919

Aobchem AOBCHEM

5001063374 2-FLUORO-5-NITROPHENYLBORONIC

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920

Aobchem AOBCHEM

5001063616 3-AMINOPHENYLBORONIC ACID PINA

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921

Frontier Specialty Chemicals 5G 1-CYCLOHEXENYLBORONIC ACID

1-Cyclohexenyl boronic acid pinacol ester; CAS No: 141091-37-4

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922

Aobchem AOBCHEM

5000950517 2 6-DIMETHYL-4-FLUOROPHENYLBOR

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923

Medchemexpress LLC Boronic acid, B-(3-aminophenyl)- | 30418-59-8 | MFCD00007755 | 99.9% | 136.94 g/mol | C6H8BNO2 | 100 G

3-Aminophenylboronic acid (m-aminophenylboronic acid) is an organoboron compound used in research and synthesis. It serves as a versatile building block in organic chemistry and as a reagent for biochemical applications, including functionalization of nanomaterials for selective glycoprotein detection.

Molecular formula C6H8BNO2 and molecular weight 136.94 g/mol.
High purity suitable for analytical and synthetic use.
Compatible with cross-coupling reactions such as Suzuki-Miyaura.
Soluble in common organic solvents and available in solution forms.
Supplied in multiple solid pack sizes for scale flexibility.
Useful for derivatization and surface functionalization of nanomaterials.

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924

Aobchem AOBCHEM

5000959272 2-CYANO-6-METHOXYPHENYLBORONIC

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925

eMolecules 950511-17-8 | m-Benzenediboronic acid pinacol ester, 1,8-diaminonaphthalene, protected | Combi-Blocks | MFCD17018842 | 370.070 | C22H24B2N2O2 | 95.000 | CC1(C)OB(OC1(C)C)c1cccc(c1)B1Nc2cccc3cccc(N1)c23 | 1g | 482933567

m-Benzenediboronic acid pinacol ester, 1,8-diaminonaphthalene, protected | Combi-Blocks | 950511-17-8 | MFCD17018842 | 370.070 | C22H24B2N2O2 | 95.000 | CC1(C)OB(OC1(C)C)c1cccc(c1)B1Nc2cccc3cccc(N1)c23 | 1g | 482933567