(3S,5R)-1-ETHYNYL-3-HYDROXY-5-([N-(6-HYDROXYHEXYL)-CARBAMOYL]-OXY)-2-METHYL-1-CYCLOHEXENE
Compound with spectra: 1 NMR
![(3S,5R)-1-ETHYNYL-3-HYDROXY-5-([N-(6-HYDROXYHEXYL)-CARBAMOYL]-OXY)-2-METHYL-1-CYCLOHEXENE](/api/compound/BQwZ79h0MnA.png?ph=true&h=300&w=458 "(3S,5R)-1-ETHYNYL-3-HYDROXY-5-([N-(6-HYDROXYHEXYL)-CARBAMOYL]-OXY)-2-METHYL-1-CYCLOHEXENE")
| SpectraBase Compound ID | BQwZ79h0MnA |
|---|---|
| InChI | InChI=1S/C16H25NO4/c1-3-13-10-14(11-15(19)12(13)2)21-16(20)17-8-6-4-5-7-9-18/h1,14-15,18-19H,4-11H2,2H3,(H,17,20)/t14-,15+/m0/s1 |
| InChIKey | NVFZLYBCQCTURI-LSDHHAIUSA-N |
| Mol Weight | 295.38 g/mol |
| Molecular Formula | C16H25NO4 |
| Exact Mass | 295.178358 g/mol |
| Enantiomer InChIKey | NVFZLYBCQCTURI-CABCVRRESA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
(3S,5R)-5-([N-BUTYLCARBAMOYL]-OXY)-1-ETHYNYL-3-HYDROXY-2-METHYL-1-CYCLOHEXENE
(3R,5S)-5-[[N-(3-AMINOPROPYL)-CARBAMOYL]-OXY]-1-ETHYNYL-3-HYDROXY-2-METHYL-1-CYCLOHEXENE
(3R,5S)/(3R,5R)-5-[[N-(3-AMINOPROPYL)-CARBAMOYL]-OXY]-1-ETHYNYL-3-HYDROXY-2-METHYL-1-CYCLOHEXENE
(3S,5R)-1-ETHYNYL-3-HYDROXY-5-([N-(2-HYDROXYETHYL)-CARBAMOYL]-OXY)-2-METHYL-1-CYCLOHEXENE
(3S,5R)-N-([(1-ETHYNYL-3-HYDROXY-2-METHYL-1-CYCLOHEXEN-5-YL)-OXY]-CARBONYL)-GYCINE
(3S,5S)/(3R,5R)-1-ETHYNYL-3-HYDROXY-2-METHYL-5-[(ACETONOXIME)-CARBONYLOXY]-1-CYCLOHEXENE
(R)-4-Ethynyl-3,5,5-trimethylcyclohex-3-enyl Acetate
Bicyclo[3.2.1]oct-6-ene, 2,8-dimethoxy-
2-[(1S,3S,5R)-5-acetoxy-3-hydroxy-2-methylene-cyclohexyl]acetic acid methyl ester
3,5-Dihydroxy-4,6-dimethylnonan-7-yl phenylcarbamate
| Title | Journal or Book | Year |
|---|---|---|
| Selective Alkoxycarbonylation of A-Ring Precursors of Vitamin D Using Enzymes in Organic Solvents. Chemoenzymatic Synthesis of 1α,25-Dihydroxyvitamin D3 C-5 A-Ring Carbamate Derivatives1 | The Journal of Organic Chemistry | 1997 |