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N-(2-hydroxyethyl)acetamide
SpectraBase Compound ID GkVy6bRUul9
InChI InChI=1S/C4H9NO2/c1-4(7)5-2-3-6/h6H,2-3H2,1H3,(H,5,7)
InChIKey PVCJKHHOXFKFRP-UHFFFAOYSA-N
Mol Weight 103.12 g/mol
Molecular Formula C4H9NO2
Exact Mass 103.063329 g/mol
Copyright Copyright © 1980, 1981-2025 John Wiley & Sons, Inc. All Rights Reserved.
Source of Sample The Richardson Company
Technique BETWEEN SALTS
Copyright Copyright © 1980, 1981-2025 John Wiley & Sons, Inc. All Rights Reserved.
Source of Sample Lipo Chemicals, Inc.
Technique NEAT
Copyright Copyright © 1980, 1981-2025 John Wiley & Sons, Inc. All Rights Reserved.
Source of Sample Scher Chemicals, Inc.
Technique NEAT
Copyright Copyright © 1980, 1981-2025 John Wiley & Sons, Inc. All Rights Reserved.
Source of Sample MCB MANUFACTURING CHEMISTS, NORWOOD, OHIO
Technique CAPILLARY CELL: NEAT
Copyright Copyright © 2018-2025 Sigma-Aldrich Co. LLC. - Database Compilation Copyright © 2018-2025 John Wiley & Sons, Inc. All Rights Reserved.
Source of Sample Aldrich
Source of Spectrum Sigma-Aldrich Co. LLC.
Catalog Number 100455
Technique Neat
Copyright Copyright © 1980, 1981-2025 John Wiley & Sons, Inc. All Rights Reserved.
Source of Sample MCB Manufacturing Chemists, Norwood, Ohio
Solvent Chloroform-d; Reference=TMS Spectrometer= Varian CFT-20
Copyright Copyright © 2002-2025 Wiley-VCH GmbH. All Rights Reserved.
Solvent CDCl3
Copyright Copyright © 2016-2025 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
Copyright Copyright © 2016-2025 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Copyright Copyright © 2016-2025 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
Copyright Copyright © 2009-2025 John Wiley & Sons, Inc. All Rights Reserved.
Solvent D2O
Copyright Copyright © 1980, 1981-2025 John Wiley & Sons, Inc. All Rights Reserved.
Copyright Copyright © 2020-2025 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum NP-0-2352-0
Copyright Copyright © 2020-2025 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum RB-1982-9364-0
Copyright Copyright © 2018-2025 Sigma-Aldrich Co. LLC. - Database Compilation Copyright © 2018-2025 John Wiley & Sons, Inc. All Rights Reserved.
Source of Sample Aldrich
Catalog Number 100455
Copyright Copyright © 2017-2025 Sigma-Aldrich Co. LLC. - Database Compilation Copyright © 2017-2025 John Wiley & Sons, Inc. All Rights Reserved.
Catalog Number 100455
  • PVCJKHHOXFKFRP-UHFFFAOYSA-N
  • Acetamide, N-(2-hydroxyethyl)-
  • Acetamide MEA
  • Lipamide MEAA
  • ACETIC MONOETHANOLAMIDE
  • INCROMECTANT AMEA
  • SCHERCOMID AME
  • MEA ACETIC ACID
  • 75% SOLUTION OF THE MONOETHANOLAMIDE OF ACETIC ACID
  • N-Acetylethanolamine
  • Amidex AME
  • Carsamide AMEA
  • Foamid AME-70
  • Foamid AME-75
  • Foamid AME-100
  • Hetamide MA
  • Incromectant AMEA-70
  • Incromectant AMEA-100
  • N-Ethanolacetamide
  • N-Acetyl-2-aminoethanol
  • Upamide acmea
  • Acetylcolamine
  • N-(.beta.-Hydroxyethyl)acetamide
  • 2-Acetamidoethanol
  • Acetic acid amide, N-(2-hydroxyethyl)-
  • Acetylethanolamine
  • 2-Acetylaminoethanol
  • Hydroxyethyl acetamide
  • .beta.-Hydroxyethylacetamide
  • N-(2-hydroxyethyl)ethanamide
  • HSDB 2713
  • EINECS 205-530-8
  • NSC 5999
  • BRN 1811708
  • AI3-02836
Title Journal or Book Year
N-Heterocyclic Carbene-Catalyzed Amidation of Unactivated Esters with Amino Alcohols Organic Letters 2005
Synthese und Eigenschaften von mit sauren und basischen Resten substituierten Hypericinen: Hypericintetrasulfonsäure – ein wasserlösliches Hypericinderivat Monatshefte fuer Chemie/Chemical Monthly 1998

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