(3S,5R)-5-([N-BUTYLCARBAMOYL]-OXY)-1-ETHYNYL-3-HYDROXY-2-METHYL-1-CYCLOHEXENE
Compound with spectra: 1 NMR
![(3S,5R)-5-([N-BUTYLCARBAMOYL]-OXY)-1-ETHYNYL-3-HYDROXY-2-METHYL-1-CYCLOHEXENE](/api/compound/KGgA9vb5n34.png?ph=true&h=300&w=458 "(3S,5R)-5-([N-BUTYLCARBAMOYL]-OXY)-1-ETHYNYL-3-HYDROXY-2-METHYL-1-CYCLOHEXENE")
| SpectraBase Compound ID | KGgA9vb5n34 |
|---|---|
| InChI | InChI=1S/C14H21NO3/c1-4-6-7-15-14(17)18-12-8-11(5-2)10(3)13(16)9-12/h2,12-13,16H,4,6-9H2,1,3H3,(H,15,17)/t12-,13+/m0/s1 |
| InChIKey | YJVPZKFKQBOXOC-QWHCGFSZSA-N |
| Mol Weight | 251.33 g/mol |
| Molecular Formula | C14H21NO3 |
| Exact Mass | 251.152144 g/mol |
| Enantiomer InChIKey | YJVPZKFKQBOXOC-OLZOCXBDSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
(3R,5S)-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
(3R,5S)-1-ETHYNYL-3-HYDROXY-2-METHYL-5-[(VINYLOXY)-CARBONYLOXY]-1-CYCLOHEXENE
(3S,5S)/(3R,5R)-1-ETHYNYL-3-HYDROXY-2-METHYL-5-[(VINYLOXY)-CARBONYLOXY]-1-CYCLOHEXENE
(R)-4-Ethynyl-3,5,5-trimethylcyclohex-3-enyl Acetate
Bicyclo[3.2.1]oct-6-ene, 2,8-dimethoxy-
3,5-Dihydroxy-4,6-dimethylnonan-7-yl phenylcarbamate
2-[(1S,3S,5R)-5-acetoxy-3-hydroxy-2-methylene-cyclohexyl]acetic acid methyl ester
cis-Methyl 2,3-Dimethyl-5-methoxy-2-cyclohexene-1-carboxylate
trans-Methyl 2,3-Dimethyl-5-methoxy-2-cyclohexene-1-carboxylate
| 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 |