1126-00-7 | 1-Phenyl-1H-pyrazole

Packsize	Purity	Availability	Price	Discounted Price
5g	98%	in stock	$12.00	$9.00
10g	98%	in stock	$17.00	$12.00
15g	98%	in stock	$21.00	$15.00
25g	98%	in stock	$30.00	$21.00

Description

• Catalog Number: AB58734
• Chemical Name: 1-Phenyl-1H-pyrazole
• CAS Number: 1126-00-7
• Molecular Formula: C9H8N2
• Molecular Weight: 144.17322
• MDL Number: MFCD00003112
• SMILES: c1ccc(cc1)n1cccn1
• NSC Number: 65588

Computed Properties

• Complexity: 119
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 11
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 1
• XLogP3: 2.2

Literature

• 1,12-diazaperylene and 2,11-dialkylated-1,12-diazaperylene iridium(III) complexes [Ir(C^N)2(N^N)]PF6: new supramolecular assemblies.

  Dalton transactions (Cambridge, England : 2003) 20120914

• (2E)-1-(2,4-Dichloro-phen-yl)-3-[3-(4-nitro-phen-yl)-1-phenyl-1H-pyrazol-4-yl]prop-2-en-1-one.

  Acta crystallographica. Section E, Structure reports online 20120301

• Long-lived room temperature deep-red/near-IR emissive intraligand triplet excited state (3IL) of naphthalimide in cyclometalated platinum(II) complexes and its application in upconversion.

  Inorganic chemistry 20111121

• New cyclometallated precursors of unsubstituted N-phenylpyrazole [{Pd(phpz)(μ-X)}2] (X = AcO or OH) and study of their reactivity towards selected ligands.

  Dalton transactions (Cambridge, England : 2003) 20110107

• Rhodium-catalyzed oxidative 1:1, 1:2, and 1:4 coupling reactions of phenylazoles with internal alkynes through the regioselective cleavages of multiple C-H bonds.

  The Journal of organic chemistry 20110107

• A study of the vaporization enthalpies of some 1-substituted imidazoles and pyrazoles by correlation-gas chromatography.

  The journal of physical chemistry. B 20101223

• Alkyne insertion into cyclometallated pyrazole and imine complexes of iridium, rhodium and ruthenium; relevance to catalytic formation of carbo- and heterocycles.

  Dalton transactions (Cambridge, England : 2003) 20101121

• Synthesis of new 2,3-dihydroquinazolin-4(1H)-one derivatives for analgesic and anti-inflammatory evaluation.

  Archiv der Pharmazie 20100501

• Zwitterionic iridium complexes: synthesis, luminescent properties, and their application in cell imaging.

  Inorganic chemistry 20100405

• Structure, photophysical and electrochemical properties, biomolecular interactions, and intracellular uptake of luminescent cyclometalated iridium(III) dipyridoquinoxaline complexes.

  Inorganic chemistry 20100301

• Temperature dependence of blue phosphorescent cyclometalated Ir(III) complexes.

  Journal of the American Chemical Society 20090722

• Synthesis of new N-phenylpyrazole derivatives with potent antimicrobial activity.

  Bioorganic & medicinal chemistry 20080415

• Regioselective synthesis and antitumor screening of some novel N-phenylpyrazole derivatives.

  Bioorganic & medicinal chemistry 20080115

• Deprotonative metalation of five-membered aromatic heterocycles using mixed lithium-zinc species.

  The Journal of organic chemistry 20080104

• Synthesis, photophysical and electrochemical properties, and protein-binding studies of luminescent cyclometalated iridium(III) bipyridine estradiol conjugates.

  Chemistry (Weinheim an der Bergstrasse, Germany) 20070101

• Heteroleptic cyclometalated iridium(III) complexes displaying blue phosphorescence in solution and solid state at room temperature.

  Inorganic chemistry 20051031

• Acute human self-poisoning with the N-phenylpyrazole insecticide fipronil--a GABAA-gated chloride channel blocker.

  Journal of toxicology. Clinical toxicology 20040101

• Synthesis and characterization of facial and meridional tris-cyclometalated iridium(III) complexes.

  Journal of the American Chemical Society 20030618

• Retention modeling and resolution optimization for a group of N-phenylpyrazole derivatives in micellar electrokinetic chromatography using empirical and physicochemical models.

  Electrophoresis 20030101

• Carbon-carbon-linked (pyrazolylphenyl)oxazolidinones with antibacterial activity against multiple drug resistant gram-positive and fastidious gram-negative bacteria.

  Bioorganic & medicinal chemistry 20011201