216485-86-8

Basic information

• Product Name: 3-ISOPROPOXYPHENYLBORONIC ACID
• Synonyms: 3-Isopropoxyphenylboronic acid ,97%;3-[(Prop-2-yl)oxy]benzeneboronic acid;[3-(propan-2-yloxy)phenyl]boronic acid;3-(1-Methylethoxy)phenylboronic acid;3-(1-Methylethyl)oxyphenylboronic acid;3-Isopropoxybenzeneboronic acid(Contains varying amounts of anhydride);3-ISOPROPOXYPHENYLBORONIC ACID;3-ISOPROPOXYBENZENEBORONIC ACID
• CAS NO: 216485-86-8
• Molecular Formula: C9H13BO3
• Molecular Weight: 180.01
• Product Categories: Boronic Acids and Derivatives;Boronate Ester;Boronic Acid;Potassium Trifluoroborate;blocks;BoronicAcids;Boronic acids;Aryl;Boronic Acids
• Mol File: 216485-86-8.mol
• Article Data: 1

Chemical Properties

• Melting Point: 76-81 °C(lit.)
• Boiling Point: 331.5 °C at 760 mmHg
• Flash Point: 110 °C
• Appearance: /
• Density: 1.1 g/cm³
• Vapor Pressure: 6.2E-05mmHg at 25°C
• Refractive Index: 1.511
• Storage Temp.: under inert gas (nitrogen or Argon) at 2-8°C
• Solubility: soluble in Methanol
• PKA: 8.24±0.10(Predicted)
• CAS DataBase Reference: 3-ISOPROPOXYPHENYLBORONIC ACID(CAS DataBase Reference)
• NIST Chemistry Reference: 3-ISOPROPOXYPHENYLBORONIC ACID(216485-86-8)
• EPA Substance Registry System: 3-ISOPROPOXYPHENYLBORONIC ACID(216485-86-8)

Safety Data

• Hazard Codes: Xi
• Safety Statements: 24/25
• WGK Germany: 3
• Hazardous Substances Data: 216485-86-8(Hazardous Substances Data)

Usage

Chemical Properties

Off-white solid

Uses

Different sources of media describe the Uses of 216485-86-8 differently. You can refer to the following data:
1. Reactant for synthesis of:Heteroaryl benzylureas with glycogen synthase kinase 3 (GSK-3) inhibitory activityModulators of survival motor neuron (SMN) proteinInhibitors of cholesteryl ester transfer protein (CETP)Selective sphingosine-1-phosphate receptor subtype-1 agonistsCytotoxic open lactone analogs of Lamellarin D
2. suzuki reaction

InChI:InChI=1/C9H13BO3/c1-7(2)13-9-5-3-4-8(6-9)10(11)12/h3-7,11-12H,1-2H3

Downstream Products

• 1609690-03-0 (S)-(3’-isopropoxy-[1,1’-biphenyl]-4-yl)methyl 2-(((S)-3-amino-1-cyano-3-oxopropyl)carbamoyl)-pyrrolidine-1-carboxylate 
• 1610518-17-6 7-(3-isopropoxyphenyl)-5-methyl-2-((4-(methylsulphonyl)piperazin-1-yl)methyl)thieno[3,2-c]pyridin-4(5H)-one 
• 1311262-35-7 2′-amino-6-(3-isopropoxyphenyl)-1′,2,2-trimethylspiro-[chroman-4,4′-imidazol]-5′(1′H)-one 
• 1390666-08-6 C₃₄H₄₃NO₅ 
• 1352136-08-3 2,7-bis(3-isopropoxyphenyl)acridine 

Relevant articles and documents

Efficiently self-healing boronic ester crystals

The perception of organic crystals being rigid static entities is quickly eroding, and molecular crystals are now matching a number of properties previously thought to be unique to soft materials. Here, we present crystals of a boronate ester that encompass many of the elastic and plastic mechanical properties of polymers such as bending, twisting, coiling and highly efficient self-healing of up to 67%, while they maintain their long-range structural order. The approach utilizes the concept of dynamic covalent chemistry and proves it can be applied towards ordered materials. This work expands our current understanding of the properties of crystalline molecular materials, and it could have implications towards the development of mechanically robust organic crystals that are capable of self-repair for durable all-organic electronics and soft robotics.