Description

Boronic acid, B-(4-formylphenyl)- (CAS No. 87199-17-5) is a high-purity boronic acid derivative with the molecular formula C₇H₇BO₃. This compound, also known as (4-formylphenyl)boronic acid, features a reactive formyl group (-CHO) and a boronic acid (-B(OH)₂) moiety, making it a versatile building block for organic synthesis, Suzuki-Miyaura cross-coupling reactions, and pharmaceutical intermediates. Its crystalline structure and stability under controlled conditions ensure consistent performance in research and industrial applications. Ideal for chemists and material scientists, this product is rigorously tested for purity (>98%) and is available in scalable quantities to meet both laboratory and production needs. Store in a cool, dry place under inert conditions to maintain optimal stability.

Properties

• CAS Number: 87199-17-5
• Complexity: 130
• IUPAC Name: (4-formylphenyl)boronic acid
• InChI: InChI=1S/C7H7BO3/c9-5-6-1-3-7(4-2-6)8(10)11/h1-5,10-11H
• InChI Key: VXWBQOJISHAKKM-UHFFFAOYSA-N
• Exact Mass: 150.0488242
• Molecular Formula: C7H7BO3
• Molecular Weight: 149.94
• SMILES: B(C1=CC=C(C=C1)C=O)(O)O
• Topological: 57.5
• Monoisotopic Mass: 150.0488242
• Synonyms: 4-Formylphenylboronic acid, 87199-17-5, 4-Formylbenzeneboronic acid, Boronic acid, (4-formylphenyl)-, p-formylphenylboronic acid, Z4V1TO2DWR, Boronic acid, B-(4-formylphenyl)-, 4-formylphenylborate, DTXSID6074887, EC 438-670-5, B-(4-FORMYLPHENYL)BORONIC ACID, DTXCID3048570, 438-670-5, 617-982-7, (4-formylphenyl)boronic acid, MFCD00151823, 4-benzaldehyde boronic acid, 4-formylphenyl boronic acid, CHEMBL140254, 4-Boronobenzaldehyde, 4-Formylphenylboronicacid, 4-formyl-phenylboronic acid, 4-(Dihydroxyboryl)benzaldehyde, 4-(Dihydroxyboranyl)Benzaldehyde, 4-formyl boronic acid, UNII-Z4V1TO2DWR, 4-formylbenzenboronic acid, 4-formylbezeneboronic acid, 4-formyl phenylboronic acid, SCHEMBL5840, 4-formylbenzene boronic acid, 4-formylbenzene-boronic acid, 4-Formyl-benzeneboronic acid, 4-formyl phenyl boronic acid, 4-Formylphenylboronic acid #, 4-(formyl)benzeneboronic acid, 4-FORMYL-BORONIC ACID, (4-formylphenyl) boronic acid, (4-formylphenyl)-boronic acid, 4-(Dihydroxyboryl)benzaldehyde; 4-Boronobenzaldehyde, SCHEMBL3718497, P-FORMYLBENZENEBORONIC ACID, 4-Formylphenylboronic acid (contains varying amounts of Anhydride), ALBB-006114, BCP26645, BDBM50067894, SBB004077, STK503716, AKOS000264729, AB03995, AS-2267, CS-W009126, 4-Formylphenylboronic acid, >=95.0%, NCGC00092013-01, NCGC00092013-02, FF117162, DB-009543, F0446, NS00019753, EN300-54979, AF-399/25108026, 4-BORONOBENZALDEHYDE~4-FORMYLPHENYLBORONIC ACID, Q28101340, F1371-0201, Z819251758

Application

Boronic acid, B-(4-formylphenyl)-, is widely used in organic synthesis as a key intermediate for Suzuki-Miyaura cross-coupling reactions, enabling the formation of biaryl compounds. Its formyl group allows further functionalization, making it valuable in the development of pharmaceuticals, agrochemicals, and advanced materials. Researchers also utilize it in the design of sensors and catalysts due to its boronic acid moiety’s affinity for diols and other Lewis bases.

Safety and Hazards

GHS Hazard Statements

• H317: May cause an allergic skin reaction [Warning Sensitization, Skin]

Precautionary Statements

• P261, P272, P280, P302+P352, P321, P333+P317, P362+P364, and P501

Hazard Classes and Categories

• Skin Corr. 1B (66.9%)
• Skin Sens. 1 (97.5%)

If you are interested or have any questions, please contact us at support@atomfair.com

Disclaimer: Sold exclusively for laboratory research. Prohibited for commercial use, diagnostics, or human/animal applications. Buyers assume all compliance liability.