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3-[(1R*,2R*)-E-ETHOXYCARBONYL-2-TRIISOPROPYLSILYLOXYMETHYL)-CYCLOHEX-5-ENYL]-PROPANOIC-ACID

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

3-[(1R*,2R*)-E-ETHOXYCARBONYL-2-TRIISOPROPYLSILYLOXYMETHYL)-CYCLOHEX-5-ENYL]-PROPANOIC-ACID
SpectraBase Compound ID Ii6eMkcOYko
InChI InChI=1S/C22H40O5Si/c1-8-26-21(25)22(14-10-9-11-19(22)12-13-20(23)24)15-27-28(16(2)3,17(4)5)18(6)7/h9,11,16-19H,8,10,12-15H2,1-7H3,(H,23,24)/t19-,22-/m1/s1
InChIKey SBVFBMNAUFEIOS-DENIHFKCSA-N
Mol Weight 412.6 g/mol
Molecular Formula C22H40O5Si
Exact Mass 412.264501 g/mol
Enantiomer InChIKey SBVFBMNAUFEIOS-UGKGYDQZSA-N

View Spectrum of 3-[(1R*,2R*)-E-ETHOXYCARBONYL-2-TRIISOPROPYLSILYLOXYMETHYL)-CYCLOHEX-5-ENYL]-PROPANOIC-ACID

MS (GC) Spectrum
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Source of Spectrum KC-0-4050-18

View Spectrum of 3-[(1R*,2R*)-E-ETHOXYCARBONYL-2-TRIISOPROPYLSILYLOXYMETHYL)-CYCLOHEX-5-ENYL]-PROPANOIC-ACID

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
  • 3-[(1S*,2S*)-2-Ethoxycarbonyl-2-(triisopropylsilyloxymethyl)cyclohex-5-enyl]propanoic acid
3-[(1S*,2R*)-2-ETHOXYCARBONYL-2-(TRIISOPROPYLSILYLMETHYL)-CYCLOHEX-5-ENYL]-PROPANOIC-ACID
2-(4-acetoxycyclohex-2-en-1-yl)-2-propargyl-malonic acid diethyl ester
Diethyl 2-[3'-(2",2",6",6"-tetramethylpiperidin-1"-yloxy)but-2'-eny]cyclopentane-1,1-dicarboxylate
Bicyclo[2.2.1]hept-5-ene-2-propanoic acid, 2-(methoxycarbonyl)-, methyl ester
Bicyclo[2.2.1]hept-5-ene-2,2-dicarboxylic acid, 2-ethyl 2-(2-methoxyethyl) ester
Bicyclo[2.2.1]hept-5-ene-2,2-dicarboxylic acid, 2-(2-chloroethyl) 2-methyl ester
Bicyclo[2.2.1]hept-5-ene-2,2-dicarboxylic acid, 2-butyl 2-(2-methoxyethyl) ester
Bicyclo[2.2.1]hept-5-ene-2,2-dicarboxylic acid, 2-methyl 2-(2-propen-1-yl) ester
Phenyl 4-[bis(ethoxycarbonyl)but-3-ynyl]-2,3,4-trideoxy-.alpha.,L-glcero-pent-2-enopyranoside
endo-2-(Methoxycarbonyl)tricyclo[3.2.1.0(2,4)]oct-6-ene
Title Journal or Book Year
Studies into the synthesis of a sub-unit of the neurotoxic alkaloid methyllycaconitine Journal of the Chemical Society, Perkin Transactions 1 1998
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