849404-37-1

Basic information

• Product Name: (3-Hydroxynaphthalen-2-yl)boronic acid
• Synonyms: (3-Hydroxynaphthalen-2-yl)boronic acid;3-Hydroxynaphthalene-2-boronic acid
• CAS NO: 849404-37-1
• Molecular Formula: C₁₀H₉BO₃
• Molecular Weight: 187.98766
• Mol File: 849404-37-1.mol

Chemical Properties

• Melting Point: 123 °C
• Boiling Point: 434.2±47.0 °C(Predicted)
• Appearance: /
• Density: 1.35±0.1 g/cm3(Predicted)
• Storage Temp.: 2-8°C
• PKA: 8.36±0.30(Predicted)
• CAS DataBase Reference: (3-Hydroxynaphthalen-2-yl)boronic acid(CAS DataBase Reference)
• NIST Chemistry Reference: (3-Hydroxynaphthalen-2-yl)boronic acid(849404-37-1)
• EPA Substance Registry System: (3-Hydroxynaphthalen-2-yl)boronic acid(849404-37-1)

Safety Data

• Hazardous Substances Data: 849404-37-1(Hazardous Substances Data)

Usage

Uses

Used in Organic Synthesis:
(3-Hydroxynaphthalen-2-yl)boronic acid is used as a reagent in organic synthesis for the formation of carbon-carbon and carbon-heteroatom bonds. Its ability to act as a potent Lewis acid allows it to catalyze various organic reactions, facilitating the formation of new chemical entities.
Used in Pharmaceutical Development:
In the pharmaceutical industry, (3-Hydroxynaphthalen-2-yl)boronic acid is utilized in the development of new drugs. Its unique structure and reactivity make it a promising candidate for the synthesis of bioactive compounds with potential therapeutic applications.
Used in Agrochemical Development:
(3-Hydroxynaphthalen-2-yl)boronic acid is also employed in the development of agrochemicals. Its reactivity and ability to form stable bonds with other molecules make it suitable for the synthesis of compounds with pesticidal or herbicidal properties.
Used in Materials Science:
In the field of materials science, (3-Hydroxynaphthalen-2-yl)boronic acid is used to develop new materials with specific properties. Its ability to form stable bonds with various elements allows for the creation of materials with tailored characteristics for specific applications.
Used in Medicinal Chemistry Research:
(3-Hydroxynaphthalen-2-yl)boronic acid has been investigated for its potential biological activities, such as anticancer and anti-inflammatory properties. Its unique structure and reactivity make it a valuable target for further research and development in the fields of medicinal and pharmaceutical chemistry, with the potential to contribute to the discovery of novel therapeutic agents.

Upstream product

• 104115-76-6 3-methoxynaphthalen-2-ylboronic acid 
• 93-04-9 2-Methoxynaphthalene 

Downstream Products

• 1027500-17-9 3-(1-benzenesulfonyl-1H-pyrrolo[2,3-b]pyridin-3-yl)-4-(3-hydroxy-naphthalen-2-yl)-1-methyl-pyrrole-2,5-dione 
• 135-19-3 β-naphthol 
• 849404-42-8 trifluoromethanesulfonic acid 3-[4-(1-benzenesulfonyl-6-benzyloxy-1H-indol-3-yl)-1-methyl-2,5-dioxo-2,5-dihydro-1H-pyrrol-3-yl]naphthalen-2-yl ester 
• 849404-41-7 trifluoromethanesulfonic acid 3-[4-(1-benzenesulfonyl-5-benzyloxy-1H-indol-3-yl)-1-methyl-2,5-dioxo-2,5-dihydro-1H-pyrrol-3-yl]naphthalen-2-yl ester 
• 849404-38-2 3-(1-benzenesulfonyl-5-benzyloxy-1H-indol-3-yl)-4-(3-hydroxy-naphthalen-2-yl)-1-methyl-pyrrole-2,5-dione 
• 849404-39-3 3-(1-benzenesulfonyl-6-benzyloxy-1H-indol-3-yl)-4-(3-hydroxy-naphthalen-2-yl)-1-methyl-pyrrole-2,5-dione 

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