CAS 137297-49-5
:(Bromomethyl)-boronic acid bis(1-methylethyl) ester
Description:
(Bromomethyl)-boronic acid bis(1-methylethyl) ester, with the CAS number 137297-49-5, is an organoboron compound characterized by the presence of a boronic acid functional group and a bromomethyl substituent. This compound typically exhibits a polar nature due to the boronic acid moiety, which can participate in hydrogen bonding and coordination with various nucleophiles. The presence of the isopropyl ester groups enhances its lipophilicity, making it more soluble in organic solvents. It is often utilized in organic synthesis, particularly in cross-coupling reactions, due to the reactivity of the boronic acid group. Additionally, the bromomethyl group can serve as a versatile electrophile, allowing for further functionalization. The compound's stability and reactivity can be influenced by environmental factors such as temperature and pH. Overall, (Bromomethyl)-boronic acid bis(1-methylethyl) ester is a valuable intermediate in the synthesis of complex organic molecules, particularly in the fields of medicinal chemistry and materials science.
Formula:C7H16BBrO2
InChI:InChI=1/C7H16BBrO2/c1-6(2)10-8(5-9)11-7(3)4/h6-7H,5H2,1-4H3
SMILES:CC(C)OB(CBr)OC(C)C
Synonyms:- Diisopropyl(bromomethyl)boronate
- Bis(1-Methylethyl) (Bromomethyl)Boronate
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Found 5 products.
Diisopropyl (Bromomethyl)boronate
CAS:Formula:C7H16BBrO2Purity:>95.0%(GC)Color and Shape:Colorless to Light yellow to Light orange clear liquidMolecular weight:222.92Diisopropyl (bromomethyl)boronate
CAS:Formula:C7H16BBrO2Purity:95.0%Color and Shape:LiquidMolecular weight:222.9157(Bromomethyl)boronic acid, bis(isopropyl) ester
CAS:<p>(Bromomethyl)boronic acid, bis(isopropyl) ester</p>Formula:C7H16BBrO2Purity:95%Color and Shape: clear. colourless liquidMolecular weight:222.92g/molDiisopropyl(bromomethyl)boronate
CAS:<p>Diisopropyl(bromomethyl)boronate is a reagent used in organic synthesis. It is an alkynyl boronic ester that reacts with alkenes to form new carbon-carbon bonds. Diisopropyl(bromomethyl)boronate can be used for the asymmetric synthesis of α,β-unsaturated carbonyl compounds and other oxidations of aldehydes and ketones. This reagent has been shown to have a high yield, solvents are not required for its preparation, and it is stable at room temperature. Diisopropyl(bromomethyl)boronate also reacts with haloalkanes and argon gas to generate organoboranes.</p>Formula:C7H16BBrO2Purity:Min. 95%Molecular weight:222.92 g/mol




