480438-72-0

Basic information

• Product Name: 2-BUTOXY-5-METHYLPHENYLBORONIC ACID
• Synonyms: A-BUTOXY-5-METHYLPHENYLBORONIC ACID;Boronic acid, (2-butoxy-5-methylphenyl)- (9CI)
• CAS NO: 480438-72-0
• Molecular Formula: C11H17BO3
• Molecular Weight: 208.06188
• Product Categories: BORONICACID;blocks;BoronicAcids;Aryl;Boronic Acids;Boronic Acids and Derivatives;Aryl Boronic Acids;Boronic Acids;Boronic Acids and Derivatives;Chemical Synthesis;Disubstituted Aryl Boronic Acids;Organometallic Reagents
• Mol File: 480438-72-0.mol

Chemical Properties

• Melting Point: 85-90 °C(lit.)
• Boiling Point: 374.5°C at 760 mmHg
• Flash Point: 180.3°C
• Appearance: /
• Density: 1.06g/cm³
• Vapor Pressure: 2.83E-06mmHg at 25°C
• Refractive Index: 1.509
• Storage Temp.: 2-8°C
• PKA: 8.68±0.53(Predicted)
• CAS DataBase Reference: 2-BUTOXY-5-METHYLPHENYLBORONIC ACID(CAS DataBase Reference)
• NIST Chemistry Reference: 2-BUTOXY-5-METHYLPHENYLBORONIC ACID(480438-72-0)
• EPA Substance Registry System: 2-BUTOXY-5-METHYLPHENYLBORONIC ACID(480438-72-0)

Safety Data

• WGK Germany: 3
• Hazardous Substances Data: 480438-72-0(Hazardous Substances Data)

Usage

Uses

Used in Pharmaceutical Research:
2-BUTOXY-5-METHYLPHENYLBORONIC ACID is used as a building block for the synthesis of various drugs and biologically active molecules due to its ability to form carbon-carbon and carbon-heteroatom bonds. Its unique reactivity and chemical structure contribute to the development of new pharmaceuticals with potential therapeutic applications.
Used in Organic Synthesis:
In the field of organic synthesis, 2-BUTOXY-5-METHYLPHENYLBORONIC ACID is used as a key intermediate for the creation of complex organic molecules. Its boronic acid functionality allows for versatile reactions, facilitating the construction of molecular frameworks that are otherwise challenging to achieve.
Used in Agrochemical Development:
2-BUTOXY-5-METHYLPHENYLBORONIC ACID is also utilized in the development of agrochemicals, where its reactivity and structural features are harnessed to create new compounds with potential applications in agriculture, such as pesticides or plant growth regulators.
Used in the Formation of Carbon-Carbon Bonds:
2-BUTOXY-5-METHYLPHENYLBORONIC ACID is employed as a reagent in the formation of carbon-carbon bonds, which are crucial for constructing the backbones of many organic molecules. Its ability to participate in such bond-forming reactions is particularly valuable in the synthesis of complex organic compounds.
Used in the Formation of Carbon-Heteroatom Bonds:
In addition to carbon-carbon bond formation, 2-BUTOXY-5-METHYLPHENYLBORONIC ACID is also used for the creation of carbon-heteroatom bonds, such as carbon-nitrogen, carbon-oxygen, and carbon-sulfur bonds. These bonds are essential for the synthesis of a wide range of organic and biologically active molecules.

InChI:InChI=1/C11H17BO3/c1-3-4-7-15-11-6-5-9(2)8-10(11)12(13)14/h5-6,8,13-14H,3-4,7H2,1-2H3