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Camalexin

Compound with spectra: 2 NMR, 2 FTIR, 1 Raman, and 2 MS (GC)

Camalexin
SpectraBase Compound ID 3sEpvrMdqsU
InChI InChI=1S/C11H8N2S/c1-2-4-10-8(3-1)9(7-13-10)11-12-5-6-14-11/h1-7,13H
InChIKey IYODIJVWGPRBGQ-UHFFFAOYSA-N
Mol Weight 200.26 g/mol
Molecular Formula C11H8N2S
Exact Mass 200.040819 g/mol

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FTIR Spectrum
Copyright Copyright © 2012-2025 John Wiley & Sons, Inc. All Rights Reserved.
Source of Sample Cayman Chemical Company
Source of Spectrum Forensic Spectral Research
Catalog Number 21971
Technique KBr0 (reground and oven dried)

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ATR-IR Spectrum
Copyright Copyright © 2019-2025 John Wiley & Sons, Inc. All Rights Reserved.
Source of Sample Cayman Chemical Company
Source of Spectrum Forensic Spectral Research
Catalog Number 21971

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13C NMR Spectrum
Copyright Copyright © 2002-2025 Wiley-VCH GmbH. All Rights Reserved.
Solvent CDCl3

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13C NMR Spectrum
Copyright Copyright © 2016-2025 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3

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Raman Spectrum
Copyright Copyright © 2015-2025 John Wiley & Sons, Inc. All Rights Reserved.
Source of Sample Cayman Chemical Company
Source of Spectrum Forensic Spectral Research
Catalog Number 21971

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MS (GC) Spectrum
Copyright Copyright © 2020-2025 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum F-51-781-7

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MS (GC) Spectrum
Copyright Copyright © 2020-2025 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum F-47-3913-5
  • 2-(1H-indol-3-yl)-1,3-thiazole
  • 1H-INDOLE, 3-(2-THIAZOLYL)-
  • 2-(1H-indol-3-yl)thiazole
  • 3-(1,3-thiazol-2-yl)-1H-indole
3-Thiophen-2-yl-1H-indole
5-(3-indolyl)-1,2,4-oxadiazole
3-(1,3,4-Oxadiazol-2-yl)-1H-indole
3-(2-furyl)-1H-indole
5-(1H-indol-3-yl)-1,3-oxazole
cyclohexanecarboxamide, N-[2-(1H-indol-3-yl)ethyl]-4-[[[(4-methylphenyl)sulfonyl]amino]methyl]-
2-amino-3-(1H-indol-3-yl)-N-(4-methylphenyl)propanamide
2-ethoxy-N-[2-(1H-indol-3-yl)ethyl]benzamide
4-besyl-N-[2-(1H-indol-3-yl)ethyl]benzamide
[(1S,6S)-6-[2-[2-(1H-indol-3-yl)ethylamino]-2-oxidanylidene-ethyl]cyclohex-3-en-1-yl]methyl ethanoate
Title Journal or Book Year
Biotransformation of the phytoalexin camalexin by the phytopathogen Rhizoctonia solani Phytochemistry 2000

This compound is available in the following databases:

KnowItAll NMR Spectral Library
Author: Wiley

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KnowItAll IR, Raman, and UV-Vis Spectral Libraries
Author: Wiley

The KnowItAll IR, Raman, and UV-Vis spectral libraries offer access to the world's largest collection of IR, Raman, and UV-Vis spectra, including the renowned Sadtler spectra. The libraries include a wide range of compounds from pure organics to industrial compounds. Learn more.

KnowItAll Mass Spectral Library
Author: Wiley

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Vendor/Supplier Catalog Number
Cayman Chemical Company
Other Resources
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