183158-33-0

Basic information

• Product Name: ACENAPHTHENE-5-BORONIC ACID
• Synonyms: Acenaphthelene-5-boronicacid;BB-8189Acenaphthene-5-boronic acid;(1,2-dihydroacenaphthylen-5-yl)boronic acid
• CAS NO: 183158-33-0
• Molecular Formula: C₁₂H₁₁BO₂
• Molecular Weight: 198.03
• Product Categories: blocks;BoronicAcids;Aryl;Boronic Acids;Boronic Acids and Derivatives
• Mol File: 183158-33-0.mol

Chemical Properties

• Melting Point: 270 °C(lit.)
• Boiling Point: 429.9°C at 760 mmHg
• Flash Point: 213.8°C
• Appearance: /
• Density: 1.28g/cm³
• Vapor Pressure: 3.74E-08mmHg at 25°C
• Refractive Index: 1.675
• Storage Temp.: under inert gas (nitrogen or Argon) at 2-8°C
• PKA: 9.11±0.20(Predicted)
• CAS DataBase Reference: ACENAPHTHENE-5-BORONIC ACID(CAS DataBase Reference)
• NIST Chemistry Reference: ACENAPHTHENE-5-BORONIC ACID(183158-33-0)
• EPA Substance Registry System: ACENAPHTHENE-5-BORONIC ACID(183158-33-0)

Safety Data

• WGK Germany: 3
• Hazardous Substances Data: 183158-33-0(Hazardous Substances Data)

Usage

Uses

Used in Organic Synthesis:
Acenaphthene-5-boronic acid is used as a reagent in organic synthesis for its ability to participate in Suzuki-Miyaura coupling reactions. This application is crucial for the creation of complex organic molecules, which are essential in various chemical and pharmaceutical processes.
Used in Pharmaceutical Research:
In the pharmaceutical industry, acenaphthene-5-boronic acid is utilized as a key building block in the development of novel drugs. Its unique structure and reactivity contribute to the design and synthesis of new drug candidates with potential therapeutic applications.
Used in Agrochemical Development:
Acenaphthene-5-boronic acid is also being explored for its potential use in the development of agrochemicals. Its properties make it a promising candidate for the creation of new compounds that can be used in agriculture for pest control and crop protection, enhancing agricultural productivity and sustainability.

InChI:InChI=1/C12H11BO2/c14-13(15)11-7-6-9-5-4-8-2-1-3-10(11)12(8)9/h1-3,6-7,14-15H,4-5H2

Upstream product

• 2051-98-1 5-bromoacenaphthene 
• 589-87-7 1,4-bromoiodobenzene 

Downstream Products

• 871320-08-0 5-(4-bromophenyl)acenaphthene 
• 198980-34-6 4,5-dihydrobenzo[l]acephenanthrylene 
• 95690-49-6 benzo[l]acephenanthrylene 
• 10047-18-4 5-acetylacenaphthene 

Relevant articles and documents

Anthracene derivative and organic electroluminescence device employing the same

An anthracene derivative with a specified asynmetrical type structure. An organic electroluminescence device which comprises at least one organic thin film layer including a light emitting layer sandwiched between a pair of electrode consisting of an anode and a cathode, wherein at least one of the organic thin film layer comprises the anthracene derivative. An organic electroluminescence device which emits blue light of enhanced purity and has a long lifetime is provided.

ANTHRACENE DERIVATIVE AND ORGANIC ELECTROLUMINESCENT DEVICE USING SAME

Disclosed is an anthracene derivative having a specific asymmetric structure. Also disclosed is an organic electroluminescent device wherein an organic thin film layer composed of one or more layers including at least a light-emitting layer is interposed between a cathode and an anode and at least one layer of the organic thin film layer contains the anthracene derivative of a specific structure by itself or as a component of a mixture. By using such an anthracene derivative, there can be realized an organic electroluminescent device having a high color purity and a long life.

Substituted phenyl farnesyltransferase inhibitors

Compounds of formula (I) or pharmaceutically acceptable salts thereof, inhibit farnesyltransferase. Methods for making the compounds, pharmaceutical compositions containing the compounds, and methods of treatment using the compounds are disclosed.