CAS 32316-92-0
:2-Naphthylboronic acid
Description:
2-Naphthylboronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a naphthalene ring. It typically appears as a white to off-white solid and is soluble in polar organic solvents such as ethanol and methanol, but less soluble in non-polar solvents. The compound is known for its ability to form reversible covalent bonds with diols, making it useful in various applications, including organic synthesis and as a reagent in Suzuki-Miyaura cross-coupling reactions. Its boronic acid functionality allows it to participate in the formation of boronate esters, which are important intermediates in organic chemistry. Additionally, 2-naphthylboronic acid has been studied for its potential applications in medicinal chemistry, particularly in the development of pharmaceuticals targeting specific biological pathways. Safety considerations include handling it with care, as boronic acids can be irritants. Overall, 2-naphthylboronic acid is a versatile compound with significant utility in both academic and industrial chemistry.
Formula:C10H9BO2
InChI:InChI=1/C10H9BO2/c12-11(13)10-6-5-8-3-1-2-4-9(8)7-10/h1-7,12-13H
InChI key:InChIKey=KPTRDYONBVUWPD-UHFFFAOYSA-N
SMILES:B(O)(O)C1=CC2=C(C=C1)C=CC=C2
Synonyms:- (2-Naphthalenyl)boronic acid
- (Naphthalene-2-yl)boronic acid
- 2-Naphthalene Boric Acid
- 2-Naphthaleneboronic acid
- 2-Naphthaleneylboronic acid
- 2-Naphthylbenzoic acid
- 2-Naphthylboric acid
- 2-Naphthylboronic acid
- 2-Naphthylboronic caid
- Akos Brn-0020
- Akos Brn-0041
- Alpha-Naphthylboric Acid
- B-2-Naphthalenylboronic acid
- Boronic acid, 2-naphthalenyl-
- Boronic acid, B-2-naphthalenyl-
- Naphthalen-2-Yl-2-Boronic Acid
- Naphthalen-2-Ylboronic Acid
- Naphthalenyl-2-Boronic Acid
- NAPHTHALENE-2-BORONIC ACID
- NAPHTHALEN-1-YLBORONIC ACID
- 1-NAPHTHALENEBORONIC ACID
- 1-NAPHTHYLBORONIC ACID
- RARECHEM AH PB 0126
- 1-NAPHTHYLENEBORONIC ACID
- NAPHTHALENE-1-BORONIC ACID
- 2-NAPHTHENEBORONIC ACID
- NAPHTHALENYL-1-BORONIC ACID
- See more synonyms
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Found 8 products.
2-Naphthaleneboronic Acid (contains varying amounts of Anhydride)
CAS:Formula:C10H9BO2Color and Shape:White to Light yellow powder to crystalMolecular weight:171.992-Naphthaleneboronic acid, 97%
CAS:<p>This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Sci</p>Formula:C10H9BO2Purity:97%Color and Shape:White to cream to pale brown, Powder or crystalline powder and/or chunksMolecular weight:171.99Naphthalene-2-boronic acid
CAS:<p>Naphthalene-2-boronic acid</p>Formula:C10H9BO2Purity:≥95%Color and Shape: white crystalline powderMolecular weight:171.99g/mol2-Naphthaleneboronic acid
CAS:Formula:C10H9BO2Purity:97%Color and Shape:Chunks,Crystalline PowderMolecular weight:171.992-Naphthaleneboronic acid
CAS:<p>2-Naphthaleneboronic acid is an organic compound that has been used as a model system for studying the binding of organic molecules to metal ions. It has been shown to bind with high affinity and specificity to sodium, potassium, and lithium ions. 2-Naphthaleneboronic acid binds to the metal ion by forming a boronate ester linkage with one of its hydroxyl groups. The other two hydroxyl groups are involved in hydrogen bonding interactions with the metal ion. This process is reversible, which allows it to be used as a model system for studying the binding of organic molecules to metal ions. 2-Naphthaleneboronic acid is also used in the synthesis of various compounds, including diphenyl ethers and anhydrous sodium carbonate. It can be prepared by reacting naphthalene with anhydrous sodium carbonate in hydrochloric acid or sodium carbonate solution at temperatures ranging from 50 °C to 150 °C</p>Formula:C10H9BO2Purity:Min. 95%Molecular weight:171.99 g/mol
