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1-Pyrenylboronic acid

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1-Pyrenylboronic acid manufacturers

  • 1-Pyrenylboronic acid
  • 1-Pyrenylboronic acid pictures
  • $30.00
  • 2022-09-23
  • CAS:164461-18-1
  • Min. Order: 1Kg
  • Purity: 99.0% up
  • Supply Ability: 20 tons per month
1-Pyrenylboronic acid Basic information
Product Name:1-Pyrenylboronic acid
Synonyms:Boronic acid, B-1-pyrenyl-;Pyrene-1-boronic acid 97%;B-1-Pyrenylboronic acid;1-Pyreneboronic Acid (contains varying amounts of Anhydride);1-Pyreneboronic acid, 1-Pyrenylboronic acid;1-Pyrenylboronic aci;1-Pyrenyboronic acid;1-Boronopyrene
CAS:164461-18-1
MF:C16H11BO2
MW:246.07
EINECS:813-398-3
Product Categories:OLED materials,pharm chemical,electronic;Aryl Boronic Acids;Boronic Acids and Derivatives;Chemical Synthesis;Organometallic Reagents;Unsubstituted Aryl Boronic Acids;fine chemicals, specialty chemicals, intermediates, electronic chemical, organic synthesis;fine chemicals, specialty chemicals, intermediates, electronic chemical, organic synthesis, functional materials;Boron Compounds;blocks;BoronicAcids;Electronic Chemicals;B (Classes of Boron Compounds);Boronic Acids;Pyrenes;OLED
Mol File:164461-18-1.mol
1-Pyrenylboronic acid Structure
1-Pyrenylboronic acid Chemical Properties
Melting point 247-251 °C(lit.)
Boiling point 509.4±33.0 °C(Predicted)
density 1.35±0.1 g/cm3(Predicted)
storage temp. Keep in dark place,Sealed in dry,Room Temperature
pka8.53±0.30(Predicted)
form Powder
color Pale yellow
Water Solubility Slightly soluble in water.
InChIInChI=1S/C16H11BO2/c18-17(19)14-9-7-12-5-4-10-2-1-3-11-6-8-13(14)16(12)15(10)11/h1-9,18-19H
InChIKeyMWEKPLLMFXIZOC-UHFFFAOYSA-N
SMILESB(C1=C2C3=C4C(C=C2)=CC=CC4=CC=C3C=C1)(O)O
CAS DataBase Reference164461-18-1(CAS DataBase Reference)
Safety Information
Safety Statements 24/25
WGK Germany 3
HS Code 29319090
Storage Class11 - Combustible Solids
MSDS Information
ProviderLanguage
SigmaAldrich English
1-Pyrenylboronic acid Usage And Synthesis
Chemical PropertiesWhite to light brown solid
UsesIt is an important raw material and intermediate used in organic synthesis agrochemical, pharmaceutical and dyestuff field. Also used as a intermediate for organic light-emitting diode(OLED).
Usessuzuki reaction
Synthesis
Trimethyl borate

121-43-7

1-Bromopyrene

1714-29-0

1-Pyrenylboronic acid

164461-18-1

The general procedure for the synthesis of 1-pyrenylboronic acid from trimethyl borate and 1-bromopyrene was as follows: 1-bromopyrene (30 g, 107 mmol) was added to a round-bottom flask and dissolved in 240 mL of tetrahydrofuran (THF). Under cooling conditions, n-BuLi (1.6 M, 80 mL) in hexane was slowly added dropwise, keeping the reaction temperature at -78 °C. After the dropwise addition was completed, the reaction mixture continued to be stirred at -78 °C for about 1 hour. Subsequently, trimethyl borate (15.5 g, 149 mmol) was added and stirring was continued at -78 °C for 1 hour. After that, the reaction mixture was warmed up to room temperature and stirred for about 2 hours. After completion of the reaction, the reaction solution was adjusted to acidic with 2N HCl. Extraction was carried out with ethyl acetate (EA) and hexane, and the organic phases were combined and concentrated under reduced pressure to remove the solvent to give 19.5 g of 1-pyrenylboronic acid in 74% yield.

References[1] Patent: KR101515814, 2015, B1. Location in patent: Paragraph 0343; 0344
[2] Patent: KR101503771, 2015, B1. Location in patent: Paragraph 0215; 0216
[3] Patent: US2014/131664, 2014, A1. Location in patent: Paragraph 0025-0026
[4] Journal of the Chemical Society, Perkin Transactions 1: Organic and Bio-Organic Chemistry (1972-1999), 1998, # 7, p. 1263 - 1268
[5] ChemPlusChem, 2013, vol. 78, # 10, p. 1288 - 1295
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