CAS 85167-10-8

1-Butylboronic acid (1S,2S,3R,5S)-(+)-2,3-pinanediol ester

Description:

1-Butylboronic acid (1S,2S,3R,5S)-(+)-2,3-pinanediol ester is a chemical compound characterized by its boronic acid functional group, which is known for its ability to form reversible covalent bonds with diols and other nucleophiles. This compound features a butyl group attached to a boron atom, enhancing its solubility and reactivity in organic synthesis. The presence of the pinanediol moiety contributes to its stereochemistry, as indicated by the specific configuration at multiple chiral centers. This stereochemical arrangement can influence the compound's reactivity and interactions in various chemical reactions, particularly in the formation of boronate esters. Additionally, boronic acids are often utilized in cross-coupling reactions, making this compound potentially valuable in organic synthesis and medicinal chemistry. Its CAS number, 85167-10-8, allows for easy identification and reference in chemical databases. Overall, this compound exemplifies the versatility of boronic acids in synthetic applications, particularly in the development of complex organic molecules.

Formula: C₁₄H₂₇BO₃

InChI: InChI=1/C14H25BO2/c1-5-6-7-15-16-12-9-10-8-11(13(10,2)3)14(12,4)17-15/h10-12H,5-9H2,1-4H3/t10-,11-,12+,14-/m0/s1

Synonyms:

• (3aS,4S,6S,7aR)-2-butyl-3a,5,5-trimethylhexahydro-4,6-methano-1,3,2-benzodioxaborole

(3aS,4S,6S,7aR)-2-Butyl-3a,5,5-trimethylhexahydro-4,6-methanobenzo[d][1,3,2]dioxaborole

CAS: 85167-10-8

Formula: C₁₄H₂₅BO₂

Color and Shape: Liquid

Molecular weight: 236.1581

Ref: IN-DA003E6M

n-Butaneboronic acid (1S,2S,3R,5S)-(+)-2,3-pinanediol ester

CAS: 85167-10-8

n-Butaneboronic acid (1S,2S,3R,5S)-(+)-2,3-pinanediol ester

Purity: ≥95%

Molecular weight: 236.16g/mol

Ref: 54-OR310106