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13-Bromo-12-methoxypodocarpa-8,11,13-trien-19-oic acid

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

13-Bromo-12-methoxypodocarpa-8,11,13-trien-19-oic acid
SpectraBase Compound ID 4O0c9Ngzg4p
InChI InChI=1S/C18H23BrO3/c1-17-7-4-8-18(2,16(20)21)15(17)6-5-11-9-13(19)14(22-3)10-12(11)17/h9-10,15H,4-8H2,1-3H3,(H,20,21)/t15?,17-,18+/m1/s1
InChIKey LAYGHFGWNZNWJY-KVJCIMDZSA-N
Mol Weight 367.28 g/mol
Molecular Formula C18H23BrO3
Exact Mass 366.083058 g/mol
Enantiomer InChIKey LAYGHFGWNZNWJY-XSRYCBBQSA-N

View Spectrum of 13-Bromo-12-methoxypodocarpa-8,11,13-trien-19-oic acid

Vapor Phase IR Spectrum
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View Spectrum of 13-Bromo-12-methoxypodocarpa-8,11,13-trien-19-oic acid

MS (GC) Spectrum
Copyright Copyright © 2020-2025 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum B-47-487-0

View Spectrum of 13-Bromo-12-methoxypodocarpa-8,11,13-trien-19-oic acid

13C NMR Spectrum
Copyright Copyright © 2016-2025 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
  • 13-bromo-12-methoxypodocarpa-8,11,13-trien-15-oic acid
  • (1S,4aS)-7-Bromo-6-methoxy-1,4a-dimethyl-1,2,3,4,4a,9,10,10a-octahydro-phenanthrene-1-carboxylic acid
  • (4beta)-13-bromo-12-methoxypodocarpa-8,11,13-trien-15-oic acid
(1S,4aS)-6-methoxy-1,4a,7-trimethyl-2,3,4,9,10,10a-hexahydrophenanthrene-1-carboxylic acid
7-Bromo-6-methoxy-1,4a-dimethyl-2,3,4,9,10,10a-hexahydrophenanthrene-1-carboxylic acid methyl ester
(1S,4aS)-6-methoxy-1,4a,7-trimethyl-2,3,4,9,10,10a-hexahydrophenanthrene-1-carboxylic acid methyl ester
INUMAKIOL-A;13-HYDROXY-12-ISOPROPYL-8,11,13-PODOCARPATRIEN-19-OIC-ACID
Gaultheric acid
13-Formyl-12-hydroxypodocarpa-8,11,13-trien-19-oic acid
1-Phenanthrenecarboxylic acid, 7-bromo-1,2,3,4,4a,9,10,10a-octahydro-6-hydroxy-1,4a-dimethyl-, methyl ester, [1S-(1.alpha.,4a.alpha.,10a.beta.)]-
LAMBERTIC ACID
METHYL-12-HYDROXY-13-IODOPODOCARPA-8,11,13-TRIEN-19-OATE
12-HYDROXY-DEHYDROABIETIC-ACID-METHYLESTER
Title Journal or Book Year
Copper(I)-Mediated Oxygenation of Diterpenoids; Three Routes to Catechol Derivatives Australian Journal of Chemistry 1994
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