213211-69-9

Basic information

• Product Name: 2-ETHOXYPHENYLBORONIC ACID
• Synonyms: RARECHEM AH PB 0149;2-ETHOXYPHENYLBORONIC ACID;2-ETHOXYBENZENEBORONIC ACID;AKOS BRN-0068;BORONIC ACID, (2-ETHOXYPHENYL)-;2-Ethoxyphenylboronic Acid (contains varying amounts of Anhydride);2-Ethoxyphenylboronic acid,98%;Ethoxyphenylboronic acid
• CAS NO: 213211-69-9
• Molecular Formula: C₈H₁₁BO₃
• Molecular Weight: 165.98
• Product Categories: blocks;BoronicAcids;Boronic Acid;B (Classes of Boron Compounds);Boronic Acids;Aryl;Boronic Acids;Boronic Acids and Derivatives;Aryl Boronic Acids;Boronic Acids and Derivatives;Chemical Synthesis;Monosubstituted Aryl Boronic Acids;Organometallic Reagents;Boronate Ester;Potassium Trifluoroborate
• Mol File: 213211-69-9.mol
• Article Data: 0

Chemical Properties

• Melting Point: 97-102 °C(lit.)
• Boiling Point: 328.8 °C at 760 mmHg
• Flash Point: 152.7 °C
• Appearance: White to off-white/Crystalline Powder or Crystals
• Density: 1.13 g/cm³
• Vapor Pressure: 7.43E-05mmHg at 25°C
• Refractive Index: 1.518
• Storage Temp.: Refrigerator (+4°C)
• Solubility: soluble in Methanol
• PKA: 8.57±0.58(Predicted)
• CAS DataBase Reference: 2-ETHOXYPHENYLBORONIC ACID(CAS DataBase Reference)
• NIST Chemistry Reference: 2-ETHOXYPHENYLBORONIC ACID(213211-69-9)
• EPA Substance Registry System: 2-ETHOXYPHENYLBORONIC ACID(213211-69-9)

Safety Data

• Hazard Codes: Xn,Xi
• Statements: 36/37/38-22
• Safety Statements: 37/39-26-36
• WGK Germany: 3
• HazardClass: IRRITANT
• Hazardous Substances Data: 213211-69-9(Hazardous Substances Data)

Usage

Chemical Properties

white to off-white crystals or crystalline powder

Uses

Different sources of media describe the Uses of 213211-69-9 differently. You can refer to the following data:
1. Reactant involved in Suzuki-Miyaura cross-coupling reactions for synthesis of pyridines and pyrimidines1, reactions of bromo-N-methylpyrrole2, or synthesis of diarylbenzophenones3Reactant involved in:? ;Ipso-amidation with nitriles4? ;Studies of the effect of biaryl phosphine ligand structure on C-N and C-C bond formation5? ;Oxidative coupling via C-H arylation6
2. suzuki reaction
3. Reactant involved in Suzuki-Miyaura cross-coupling reactions for synthesis of pyridines and pyrimidines, reactions of bromo-N-methylpyrrole, or synthesis of diarylbenzophenonesReactant involved in:Ipso-amidation with nitrilesStudies of the effect of biaryl phosphine ligand structure on C-N and C-C bond formationOxidative coupling via C-H arylation

InChI:InChI=1/C8H11BO3/c1-2-12-8-6-4-3-5-7(8)9(10)11/h3-6,10-11H,2H2,1H3

Upstream product

• 92838-43-2 Hg(C₆H₄-2-OC₂H₅)2 
• 688-74-4 boric acid tributyl ester 
• 41842-29-9 2-ethoxyphenylmagnesium bromide 
• 7732-18-5 water 

Downstream Products

• 1335222-91-7 C₁₆H₁₆N₄O 
• 1008-89-5 2-phenylpyridine 
• 89466-08-0 2-hydroxyphenyl boronic acid