CAS 138008-97-6
:2-ISOPROPOXYPHENYLBORONIC ACID
Description:
2-Isopropoxyphenylboronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a phenyl ring that is further substituted with an isopropoxy group. This compound typically exhibits properties common to boronic acids, such as the ability to form reversible complexes with diols, making it useful in various applications, including organic synthesis and medicinal chemistry. The isopropoxy group enhances its solubility in organic solvents and may influence its reactivity and stability. 2-Isopropoxyphenylboronic acid is often utilized in Suzuki-Miyaura cross-coupling reactions, which are pivotal in the formation of carbon-carbon bonds. Additionally, its boronic acid moiety can participate in the formation of boronate esters, further expanding its utility in synthetic pathways. The compound is generally handled with care due to the potential reactivity of boronic acids, particularly in the presence of moisture, which can lead to hydrolysis. Overall, 2-isopropoxyphenylboronic acid is a versatile reagent in the field of organic chemistry.
Formula:C9H13BO3
InChI:InChI=1/C9H13BO3/c1-7(2)13-9-6-4-3-5-8(9)10(11)12/h3-7,11-12H,1-2H3
SMILES:CC(C)Oc1ccccc1B(O)O
Synonyms:- 2-Isopropoxybenzeneboronic Acid
- Akos Brn-0366
- 2-Isopropoxybenzeneboronic acid 95%
- [2-(1-Methylethoxy)Phenyl]Boronic Acid
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Found 3 products.
Boronic acid, B-[2-(1-methylethoxy)phenyl]-
CAS:Formula:C9H13BO3Purity:97%Color and Shape:SolidMolecular weight:180.00872-Isopropoxybenzeneboronic acid
CAS:<p>2-Isopropoxybenzeneboronic acid</p>Purity:99%Molecular weight:180.01g/mol2-Isopropoxyphenylboronic acid
CAS:Formula:C9H13BO3Purity:95%Color and Shape:Liquid, ViscousMolecular weight:180.01


