(3S,5R)-N-([(1-ETHYNYL-3-HYDROXY-2-METHYL-1-CYCLOHEXEN-5-YL)-OXY]-CARBONYL)-GYCINE
Compound with spectra: 1 NMR
![(3S,5R)-N-([(1-ETHYNYL-3-HYDROXY-2-METHYL-1-CYCLOHEXEN-5-YL)-OXY]-CARBONYL)-GYCINE](/api/compound/KWKUNSy3egv.png?ph=true&h=300&w=458 "(3S,5R)-N-([(1-ETHYNYL-3-HYDROXY-2-METHYL-1-CYCLOHEXEN-5-YL)-OXY]-CARBONYL)-GYCINE")
| SpectraBase Compound ID | KWKUNSy3egv |
|---|---|
| InChI | InChI=1S/C12H15NO5.Na/c1-3-8-4-9(5-10(14)7(8)2)18-12(17)13-6-11(15)16;/h1,9-10,14H,4-6H2,2H3,(H,13,17)(H,15,16);/q;+1/p-1/t9-,10+;/m0./s1 |
| InChIKey | MLIUUVHQQMYODE-BAUSSPIASA-M |
| Mol Weight | 275.24 g/mol |
| Molecular Formula | C12H14NNaO5 |
| Exact Mass | 275.076967 g/mol |
| Parent InChIKey | UTVJIGSUMREFDR-VHSXEESVSA-M |
| Enantiomer InChIKey | MLIUUVHQQMYODE-UXQCFNEQSA-M |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CD3OD |
(3S,5R)-1-ETHYNYL-3-HYDROXY-5-([N-(2-HYDROXYETHYL)-CARBAMOYL]-OXY)-2-METHYL-1-CYCLOHEXENE
(3S,5R)-5-([N-BUTYLCARBAMOYL]-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
(3R,5S)-5-[[N-(3-AMINOPROPYL)-CARBAMOYL]-OXY]-1-ETHYNYL-3-HYDROXY-2-METHYL-1-CYCLOHEXENE
(3S,5R)-1-ETHYNYL-3-HYDROXY-5-([N-(6-HYDROXYHEXYL)-CARBAMOYL]-OXY)-2-METHYL-1-CYCLOHEXENE
(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 |