CAS 162662-27-3
:[4-(Methoxymethoxy)phenyl]-boronic acid
Description:
[4-(Methoxymethoxy)phenyl]-boronic acid, with the CAS number 162662-27-3, is an organoboron compound characterized by the presence of a boronic acid functional group attached to a phenyl ring that is further substituted with a methoxymethoxy group. This compound typically exhibits properties such as good solubility in organic solvents and moderate stability under standard conditions. The boronic acid moiety allows for participation in various chemical reactions, including Suzuki coupling, which is significant in organic synthesis and materials science. The methoxymethoxy substituent enhances the compound's reactivity and solubility, making it useful in medicinal chemistry and the development of pharmaceuticals. Additionally, boronic acids are known for their ability to form reversible complexes with diols, which can be exploited in sensor applications and drug delivery systems. Overall, [4-(Methoxymethoxy)phenyl]-boronic acid serves as a versatile building block in synthetic chemistry, with potential applications in various fields, including organic synthesis and materials science.
Formula:C8H11BO3
InChI:InChI=1/C8H11BO3/c1-12-6-7-2-4-8(5-3-7)9(10)11/h2-5,10-11H,6H2,1H3
SMILES:COCc1ccc(cc1)B(O)O
Synonyms:- 4-(Methoxymethyl)phenylboronic acid
- [4-(Methoxymethyl)Phenyl]Boronic Acid
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Found 3 products.
Boronic acid, B-[4-(methoxymethoxy)phenyl]-
CAS:Formula:C8H11BO4Purity:98%Color and Shape:SolidMolecular weight:181.98154-(Methoxymethoxy)phenylboronic acid
CAS:4-(Methoxymethoxy)phenylboronic acidPurity:98%Color and Shape:SolidMolecular weight:181.98g/mol(4-(Methoxymethoxy)phenyl)boronic acid
CAS:Formula:C8H11BO4Purity:98%Color and Shape:SolidMolecular weight:181.98


