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Detail of "123324-71-0"

  • CAS Number:
  • 123324-71-0
  • Name:

  • 4-tert-Butylphenylboronic acid

  • Molecular Structure:
  • Formula:
  • C10H15BO2
  • Molecular Weight:
  • 178.04
  • Synonyms:
  • 4-t-Butylphenylboronic acid;4-tert-Butyl-phenyl boronic acid;(4-t-Butylphenyl)boronic acid;4-(tert-Butyl)Phenylboronic Acid;4-Tertbutylphenylboronic Acid;4-tert-butylphenyl boronic acid;4-tert-butylphenyl boronic acid;4-tert-Butylbenzeneboronic acid; 4-(tert-Butyl)phenylboronic acid;4-(tert-Butyl)benzeneboronic acid;4-tert-Butylbenzene boronic acid;
  • Density:
  • 1.02 g/cm2
  • Melting Point:
  • 193-199 ºC
  • Boiling Point:
  • 296.7 ºC at 760 mmHg
  • Flash Point:
  • 133.2 ºC
  • Appearance:
  • white to off-white crystalline powder
  • Hazard Symbols:
  • IrritantXi
  • Risk Codes:
  • 36/37/38
  • Safety:
  • 26-37/39 Details
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CAS No.123324-71-0 4-tert-Butylphenylboronic acid

4-tert-Butylphenylboronic acid Name 4-tert-Butylphenylboronic acid Synonyms 4-tert-Butylbenzeneboronic acid; 4-(tert-Butyl)phenylboronic acid Molecular Formula C10H15BO2 Molecular Weight 178.04 CAS Registry Number 123324-71-0 Properties Melting poin

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Reference

Synthesis of N,N,N',N'-tetrasubstituted 1,3-bis(4-aminophenyl)azulenes and their application to a hole-injecting material in organic electroluminescent devices
All Rights Reserved. Synthesis of N,N,N',N'-tetrasubstituted 1,3-bis(4-aminophenyl)azulenes and their application to a hole-injecting material in organic electroluminescent devices. Thanh, Nguyen Chung; Ikai, Masamichi; Kajioka, Takanori; Fujikawa, Hisayoshi; Taga, Yasunori; Zhang, Yanmei; Ogawa, Satoshi; Shimada, Hiroko; Miyahara, Yosuke; Kuroda, Shigeyasu; Oda, Mitsunori ( Department of Applied Chemistry, Faculty of Engineering, University of Toyama, Toyama 930-8555, Japan). Tetrahedron, 62(48), 11227-11239 (English) 2006 Elsevier Ltd. CODEN: TETRAB. ISSN: 0040-4020. DOCUMENT TYPE: Journal CA Section: 73 (Optical, Electron, and Mass Spectroscopy and Other Related Properties) Section cross-reference(s): 24 After a preliminary search of the reaction conditions for the Suzuki-Miyaura cross-coupling of haloazulenes with arylboronic acids, the title compds. were synthesized either by the direct coupling reaction between 1,3-dihaloazulene and the corresponding N,N-disubstituted 4-aminophenylboronic acids or by a two-step sequence involving the cross-coupling with 4-bromophenylboronic acid and subsequent Pd-catalyzed amination. Application of the title diamines to a hole-injecting material in org. electroluminescent devices was carried out to provide their prominent characteristics as a novel durable, non-cyanine and non-polyamine substance without color fade. The diamine derivs. 123324-71-0 which is the cas registry number of one of substances is just one of reagents here., extended by an ethynyl unit between the azulenyl core and the 4-aminophenyl moiety, were also synthesized and found, unfortunately, unsuitable for vacuum deposition in prepg. a multilayer composite. .
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