150-61-8 | 1,2-Dianilinoethane

Packsize	Purity	Availability	Price	Discounted Price
250mg	95%	in stock	$15.00	$10.00
1g	98%	in stock	$15.00	$11.00
5g	98%	in stock	$29.00	$20.00
25g	98%	in stock	$82.00	$57.00

Description

• Catalog Number: AB43101
• Chemical Name: 1,2-Dianilinoethane
• CAS Number: 150-61-8
• Molecular Formula: C14H16N2
• Molecular Weight: 212.2902
• MDL Number: MFCD00003019
• SMILES: C(Nc1ccccc1)CNc1ccccc1
• NSC Number: 8719

Computed Properties

• Complexity: 150
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 16
• Hydrogen Bond Acceptor Count: 2
• Hydrogen Bond Donor Count: 2
• Rotatable Bond Count: 5
• XLogP3: 3.6

Literature

• Preparation of 1-C-glycosyl aldehydes by reductive hydrolysis.

  Carbohydrate research 20110906

• Effect of electronic structure on the photoinduced ligand exchange of Ru(II) polypyridine complexes.

  Inorganic chemistry 20110516

• Effects of 25-hydroxyvitamin D(3) on proliferation and osteoblast differentiation of human marrow stromal cells require CYP27B1/1α-hydroxylase.

  Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research 20110501

• Synthesis and chromatographic evaluation of new polymeric chiral stationary phases based on three (1S,2S)-(-)-1,2-diphenylethylenediamine derivatives in HPLC and SFC.

  Analytical and bioanalytical chemistry 20110301

• Enantioselective Michael addition of ketones to maleimides catalyzed by bifunctional monosulfonyl DPEN salt.

  Chemical communications (Cambridge, England) 20100707

• Preparation and enantioseparation of a mixed selector chiral stationary phase derived from benzoylated tartaric acid and 1,2-diphenylethylenediamine.

  Chirality 20100601

• Selective formation of cis-diacyl, cis-PPh(2)R rhodium(III) complexes by the reaction of rhodium(III) cis-diacyl, trans-PPh(2)R complexes with aliphatic diamines.

  Dalton transactions (Cambridge, England : 2003) 20091128

• Synthesis and characterization of some chiral metal-salen complexes bearing a ferrocenophane substituent.

  Molecules (Basel, Switzerland) 20091026

• Synthesis of dendritic stationary phases with surface-bonded L-phenylalanine derivate as chiral selector and their evaluation in HPLC resolution of racemic compounds.

  Chirality 20080701

• Tuning mechanism in a two-component columnar host system composed of 1,2-diphenylethylenediamine and 1,1'-binaphthyl-2,2'-dicarboxylic acid.

  Organic letters 20080207

• Synthesis of polymer-type chiral stationary phases and their enantioseparation evaluation by high-performance liquid chromatography.

  Chirality 20070201

• Successive optical resolution of two compounds by one enantiopure compound.

  Chemical communications (Cambridge, England) 20060314

• Preparation of polymer-supported Ru-TsDPEN catalysts and use for enantioselective synthesis of (S)-fluoxetine.

  Organic & biomolecular chemistry 20050721

• Determination of serotonin, noradrenaline, dopamine and their metabolites in rat brain extracts and microdialysis samples by column liquid chromatography with fluorescence detection following derivatization with benzylamine and 1,2-diphenylethylenediamine.

  Journal of chromatography. B, Analytical technologies in the biomedical and life sciences 20040805

• Simultaneous determination of 5-hydroxyindoles and catechols by high-performance liquid chromatography with fluorescence detection following derivatization with benzylamine and 1,2-diphenylethylenediamine.

  Journal of chromatography. A 20030919

• Spectrofluorometric determination of catechins with 1,2-diphenylethylenediamine.

  Analytical sciences : the international journal of the Japan Society for Analytical Chemistry 20020801