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Atomfair Cyclohexylboronic Acid (contains varying amounts of Anhydride) C6H13BO2
Description Cyclohexylboronic Acid (contains varying amounts of Anhydride) is a highly versatile organoboron compound with the molecular formula C6H13BO2. This reagent is widely utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, due to its ability to form stable boronate esters with various electrophiles. The product may contain varying amounts of its anhydride form, which does not compromise its reactivity in most applications. With a CAS number 21717-96-4 , this compound is characterized by its white to off-white crystalline appearance and should be stored under inert conditions to maintain stability. Ideal for researchers and chemists working in pharmaceutical, agrochemical, and…
Description
Description
Cyclohexylboronic Acid (contains varying amounts of Anhydride) is a highly versatile organoboron compound with the molecular formula C6H13BO2. This reagent is widely utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, due to its ability to form stable boronate esters with various electrophiles. The product may contain varying amounts of its anhydride form, which does not compromise its reactivity in most applications. With a CAS number 21717-96-4, this compound is characterized by its white to off-white crystalline appearance and should be stored under inert conditions to maintain stability. Ideal for researchers and chemists working in pharmaceutical, agrochemical, and material science fields, this boronic acid derivative offers high purity and consistent performance in C-C bond-forming reactions.
- CAS No: 21717-96-4
- Molecular Formula: C6H13BO2
- Molecular Weight: 127.98
- Exact Mass: 128.1008598
- Monoisotopic Mass: 128.1008598
- IUPAC Name: cyclohexylboronic acid
- SMILES: B(C1CCCCC1)(O)O
- Synonyms: Cyclohexylboronic Acid (contains varying amounts of Anhydride), 672-297-0, Cyclohexylboronic acid, 4441-56-9, Boronic acid, cyclohexyl-
Application
Cyclohexylboronic Acid is primarily employed in Suzuki-Miyaura cross-coupling reactions to synthesize biaryl and alkyl-aryl compounds, pivotal in drug discovery and material science. It serves as a key intermediate in the preparation of cyclohexyl-substituted aromatic systems, which are common motifs in bioactive molecules. The compound is also used in the development of boron-containing polymers and as a reagent in asymmetric synthesis.
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