CAS 7547-97-9

(1E)-prop-1-en-1-ylboronic acid

Description:

(1E)-prop-1-en-1-ylboronic acid, also known as allylboronic acid, is an organoboron compound characterized by the presence of a boronic acid functional group attached to an allyl group. This compound typically appears as a colorless to pale yellow liquid or solid, depending on its form and purity. It is soluble in water and organic solvents, making it versatile for various chemical reactions. The boronic acid moiety allows for participation in reactions such as Suzuki coupling, which is valuable in organic synthesis for forming carbon-carbon bonds. Additionally, the presence of the double bond in the allyl group provides reactivity, enabling further transformations. (1E)-prop-1-en-1-ylboronic acid is often used in medicinal chemistry and materials science due to its ability to form stable complexes with diols and its utility in the synthesis of complex organic molecules. Safety precautions should be taken when handling this compound, as boronic acids can be irritants and may pose environmental hazards.

Formula: C₃H₇BO₂

InChI: InChI=1/C3H7BO2/c1-2-3-4(5)6/h2-3,5-6H,1H3/b3-2+

InChI key: CBMCZKMIOZYAHS-NSCUHMNNSA-N

SMILES: B(/C=C/C)(O)O

trans-1-Propen-1-yl-boronic acid

CAS: 7547-97-9

trans-1-Propen-1-yl-boronic acid

Formula: C₃H₇BO₂

Purity: 98%

Molecular weight: 85.89748

Ref: 54-OR361670

trans-1-Propen-1-yl-boronic acid

CAS: 7547-97-9

Formula: C₃H₇BO₂

Purity: 98%

Color and Shape: Solid

Molecular weight: 85.8975

Ref: IN-DA0032DC

trans-1-Propen-1-yl-boronic acid

CAS: 7547-97-9

Trans-1-propenylboronic acid is a boronic acid that can be used to synthesize chiral compounds. It is a product of the Sharpless asymmetric dihydroxylation reaction and has been shown to inhibit the activity of aldehyde oxidase. Trans-1-propenylboronic acid is reusable, which makes it an economical alternative to other boronic acids. The enantiomer of trans-1-propenylboronic acid can be obtained by the Suzuki coupling reaction with a variety of different electrophiles. This product also forms hydrogen bonds with the substrate and has shown anti-inflammatory effects in mice. Trans-1-propenylboronic acid can also undergo oxidation, reduction, or cyclization reactions and can form monosubstituted alicyclic products.

Formula: C₃H₇BO₂

Purity: Min. 95%

Color and Shape: Solid

Molecular weight: 85.9 g/mol

Ref: 3D-FT160654

(E)-Prop-1-en-1-ylboronic acid

CAS: 7547-97-9

(E)-Prop-1-en-1-ylboronic acid

Formula: C₃H₇BO₂

Purity: 98%

Molecular weight: 85.9

Ref: IN-DG225076