CAS 103989-84-0
:2-METHYLNAPHTHALENE-1-BORONIC ACID
Description:
2-Methyl-naphthalene-1-boronic acid is an organic compound characterized by the presence of a boronic acid functional group attached to a naphthalene ring, specifically at the 1-position, with a methyl group at the 2-position. This compound typically appears as a white to off-white solid and is soluble in organic solvents such as ethanol and dimethyl sulfoxide (DMSO), but has limited solubility in water due to its hydrophobic naphthalene structure. The boronic acid moiety is known for its ability to form reversible covalent bonds with diols, making it valuable in various applications, including organic synthesis and materials science. It is often utilized in Suzuki coupling reactions, which are important for the formation of carbon-carbon bonds in the synthesis of complex organic molecules. Additionally, 2-methyl-naphthalene-1-boronic acid may exhibit interesting electronic properties due to the conjugated naphthalene system, potentially making it useful in the development of organic semiconductors or sensors. Safety data should be consulted for handling and storage, as with all chemical substances.
Formula:C11H11BO2
InChI:InChI=1/C11H11BO2/c1-8-6-7-9-4-2-3-5-10(9)11(8)12(13)14/h2-7,13-14H,1H3
SMILES:Cc1ccc2ccccc2c1B(O)O
Synonyms:- (2-Methyl-1-naphthyl)boronic acid
- boronic acid, B-(2-methyl-1-naphthalenyl)-
- (2-Methylnaphthalen-1-Yl)Boronic Acid
- 2-METHYLPHTHALENE-1-BORONIC ACID
- [2-METHYLPHTHALENE-1-BORONIC ACID]
- 2-Methyl-1-naphthylboronic acid
- ene-1-boronic acid
- 2-METHYLNAPHTHALENE-1-BORONIC ACID
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Found 3 products.
(2-Methylnaphthalen-1-yl)boronic acid
CAS:Formula:C11H11BO2Purity:97%Color and Shape:SolidMolecular weight:186.0148(2-methylnaphthalen-1-yl)boronic acid
CAS:(2-methylnaphthalen-1-yl)boronic acidPurity:98%Molecular weight:186.01g/mol(2-Methylnaphthalen-1-yl)boronic acid
CAS:Formula:C11H11BO2Purity:97%Color and Shape:SolidMolecular weight:186.02
