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N,O-Bis(tert-butoxycarbonyl)hydroxylamine

Compound with spectra: 4 NMR, and 1 FTIR

N,O-Bis(tert-butoxycarbonyl)hydroxylamine
SpectraBase Compound ID 1l9metaEJra
InChI InChI=1S/C10H19NO5/c1-9(2,3)14-7(12)11-16-8(13)15-10(4,5)6/h1-6H3,(H,11,12)
InChIKey AGOSGCWATIJZHQ-UHFFFAOYSA-N
Mol Weight 233.26 g/mol
Molecular Formula C10H19NO5
Exact Mass 233.126323 g/mol

View Spectrum of N,O-Bis(tert-butoxycarbonyl)hydroxylamine

13C NMR Spectrum
Copyright Copyright © 1980, 1981-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Sample Fluka AG, Buchs, Switzerland
Solvent Chloroform-d; Reference=TMS Spectrometer= Varian CFT-20

View Spectrum of N,O-Bis(tert-butoxycarbonyl)hydroxylamine

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3

View Spectrum of N,O-Bis(tert-butoxycarbonyl)hydroxylamine

13C NMR Spectrum
Copyright Copyright © 2021-2024 Sigma-Aldrich Co. LLC. - Database Compilation Copyright © 2021 John Wiley & Sons, Inc. All Rights Reserved.
Source of Sample Sigma-Aldrich Co. LLC.
Source of Spectrum Sigma-Aldrich Co. LLC.
Catalog Number 412791
Solvent CDCl3

View Spectrum of N,O-Bis(tert-butoxycarbonyl)hydroxylamine

1H NMR Spectrum
Copyright Copyright © 2021-2024 Sigma-Aldrich Co. LLC. - Database Compilation Copyright © 2021 John Wiley & Sons, Inc. All Rights Reserved.
Source of Sample Sigma-Aldrich Co. LLC.
Source of Spectrum Sigma-Aldrich Co. LLC.
Catalog Number 412791
Solvent CDCl3

View Spectrum of N,O-Bis(tert-butoxycarbonyl)hydroxylamine

FTIR Spectrum
Copyright Copyright © 2018-2024 Sigma-Aldrich Co. LLC. - Database Compilation Copyright © 2018-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Sample Aldrich
Source of Spectrum Sigma-Aldrich Co. LLC.
Catalog Number 412791
Technique Mull
  • HYDROXYCARBAMIC ACID, tert-BUTYL ESTER, tert-BUTYL CARBONATE(ESTER)
  • CARBAMIC ACID, HYDROXY-, tert-BUTYL ESTER, tert-BUTYL CARBONATE (ESTER)
  • N,O-Di-Boc-hydroxylamine
  • tert-Butyl N-(tert-butoxycarbonyloxy)carbamate
N,O-DI-TERT.-BUTOXYCARBONYL-[(15)N,(18)O]-HYDROXYLAMINE
N,O-DI-TERT.-BUTOXYCARBONYL-[(15)N,(16)O]-HYDROXYLAMINE
N-(2-Carboxy-ethoxy)-carbamic acid, tert-butyl ester
t-Butyl N-[4-[3'-(Aminopropyl)-(15N)-amino]butyl}carbamate
tert-butyl N-[3-[4-(3-aminopropoxy)butoxy]propyl]carbamate
[3-(TERT.-BUTOXYCARBONYLAMINO)-PROPYL]-PHOSPHINIC-ACID
DI-(TERT.-BUTYL)-N,N'-(4,9-DIAZADODECAN-1,12-DIYL)-BIS-CARBAMATE
N-[(1S)-1-(chloromethyl)propyl]carbamic acid tert-butyl ester
N-(2-cyanopropyl)carbamic acid tert-butyl ester
2-Bromo-N-[3-(t-butoxycarbonyl)aminopropyl]acetamide
(R)-N-TERT.-BUTYLOXYCARBONYL-3-AMINOPENTANITRILE
tert-Butyl 2-fluoro-3-hydroxypropylcarbamate
Title Journal or Book Year
Synthesis of the A/E/F sections of conaconitine, napelline and related diterpenoid alkaloids of the aconitine group Journal of the Chemical Society, Perkin Transactions 1 1998
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