1,3,4,5,6-PENTA-O-BENZYL-2-C-TRICHLOROMETHYL-MYO-INOSITOL
Compound with spectra: 1 NMR
| SpectraBase Compound ID | 35f7JVWKSOG |
|---|---|
| InChI | InChI=1S/C42H41Cl3O6/c43-42(44,45)41(46)39(50-29-34-22-12-4-13-23-34)37(48-27-32-18-8-2-9-19-32)36(47-26-31-16-6-1-7-17-31)38(49-28-33-20-10-3-11-21-33)40(41)51-30-35-24-14-5-15-25-35/h1-25,36-40,46H,26-30H2/t36-,37-,38+,39+,40-,41+ |
| InChIKey | IDKOLYCLYUPSOR-LNQZRZQPSA-N |
| Mol Weight | 748.1 g/mol |
| Molecular Formula | C42H41Cl3O6 |
| Exact Mass | 746.196872 g/mol |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | D2O |
METHYL-2,3-DI-O-BENZYL-6-DEOXY-4-C-TRICHLOROMETHYL-BETA-D-GALACTOPYRANOSIDE
2-AMINO-1,3,4,5,6-PENTA-O-BENZYL-2-C-CYANO-2-DEOXY-MYO-INOSITOL
(3aR,4S,5R,6R,7aR)-4,5-bis(phenylmethoxy)-6-(phenylmethoxymethyl)spiro[3a,4,5,6,7,7a-hexahydro-1,3-benzodioxole-2,1'-cyclohexane]
JWXHKWBUBUUEFP-OQIMXIDESA-N
JWXHKWBUBUUEFP-SNSGHMKVSA-N
2,3,4,7-TETRA-O-BENZYL-2-EPI-5-EPI-[6-(2)H(2)]-VALIOLONE
4,5,7,8-TETRA-O-BENZYL-3-BENZYLOXYCARBONYLAMINO-2,3-DIDEOXY-1-C-PHENYL-D-GLYCERO-D-IDO-1-OCTULOSE
1,6-ANHYDRO-TRI-O-BENZYL-5-HYDROXY-BETA-L-IDOPYRANOSIDE
[3AR-(3A-ALPHA,4-ALPHA,5-BETA,6-BETA,6A-BETA)]-5-(BENZOYLOXY)-6-(BENZYLOXY)-HEXAHYDRO-4-(1,1'-DIMETHOXYMETHYL)-2H-CYCLOPENTA-[B]-FURAN-2-ONE
2,3,4,6-TETRA-O-BENZYL-1-DEOXY-1-HYDRAZI-D-GALACTOPYRANOSE
| Title | Journal or Book | Year |
|---|---|---|
| An Expansion of the Role of the Corey - Link Reaction for the Synthesis of α-Substituted Carboxylic Acid Esters | Australian Journal of Chemistry | 2006 |
This compound is available in the following databases:
KnowItAll NMR Spectral Library
Author: Wiley
The KnowItAll NMR Spectral Library offers a comprehensive collection of NMR reference spectra, including NMR, CNMR, and XNMR, and covers a wide range of compounds including organics, polymers, monomers, metabolites, and more. Learn more.