CAS 1246633-36-2
:4-Chloro-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzaldehyde
Description:
4-Chloro-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzaldehyde is an organic compound characterized by its functional groups and structural features. It contains a benzaldehyde moiety, which is indicative of its aromatic nature and contributes to its reactivity, particularly in electrophilic substitution reactions. The presence of a chloro substituent enhances its electrophilic character, while the dioxaborolane group introduces boron, which can participate in various chemical transformations, including cross-coupling reactions. This compound is likely to be soluble in organic solvents due to its non-polar aromatic structure, while the boron-containing group may impart some polar characteristics. Its unique structure makes it a valuable intermediate in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. Additionally, the presence of the dioxaborolane group suggests potential applications in boron chemistry, including the formation of organoboron compounds, which are useful in various synthetic methodologies. Overall, this compound exemplifies the intersection of aromatic chemistry and organoboron chemistry, making it a subject of interest in synthetic organic chemistry.
Formula:C13H16BClO3
InChI:InChI=1S/C13H16BClO3/c1-12(2)13(3,4)18-14(17-12)11-7-10(15)6-5-9(11)8-16/h5-8H,1-4H3
InChI key:InChIKey=ZVDSWJQOVVRVKE-UHFFFAOYSA-N
SMILES:C(=O)C1=C(B2OC(C)(C)C(C)(C)O2)C=C(Cl)C=C1
Synonyms:- Benzaldehyde, 4-chloro-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-
- 4-Chloro-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzaldehyde
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Found 2 products.
5-Chloro-2-formylphenylboronic acid,pinacol ester
CAS:Formula:C13H16BClO3Purity:97%Color and Shape:SolidMolecular weight:266.52835-Chloro-2-formylphenylboronic acid pinacol ester
CAS:<p>Versatile small molecule scaffold</p>Formula:C13H16BClO3Purity:Min. 95%Molecular weight:266.53 g/mol

