#61B;MAJOR+MINOR;[(3-[(1S,4S,5R)-4-[4-(HYDROXYMETHYL)-PHENYL]-3-(TRIFLUOROMETHYLSULFONYL)-3-AZABICYCLO-[3.1.0]-HEXAN-1-YL]-5,6-DIHYDROPYRIDIN-1(2H)-(ISOXAZOL-5
Compound with spectra: 1 NMR
![#61B;MAJOR+MINOR;[(3-[(1S,4S,5R)-4-[4-(HYDROXYMETHYL)-PHENYL]-3-(TRIFLUOROMETHYLSULFONYL)-3-AZABICYCLO-[3.1.0]-HEXAN-1-YL]-5,6-DIHYDROPYRIDIN-1(2H)-(ISOXAZOL-5](/api/compound/Hch7IX08VMZ.png?ph=true&h=300&w=458 "#61B;MAJOR+MINOR;[(3-[(1S,4S,5R)-4-[4-(HYDROXYMETHYL)-PHENYL]-3-(TRIFLUOROMETHYLSULFONYL)-3-AZABICYCLO-[3.1.0]-HEXAN-1-YL]-5,6-DIHYDROPYRIDIN-1(2H)-(ISOXAZOL-5")
| SpectraBase Compound ID | Hch7IX08VMZ |
|---|---|
| InChI | InChI=1S/2C22H22F3N3O5S/c2*23-22(24,25)34(31,32)28-13-21(10-17(21)19(28)15-5-3-14(12-29)4-6-15)16-2-1-9-27(11-16)20(30)18-7-8-26-33-18/h2*2-8,17,19,29H,1,9-13H2/t2*17-,19+,21+/m00/s1 |
| InChIKey | DROUKDWQTHEUBY-RRMCILSDSA-N |
| Mol Weight | 994.98 g/mol |
| Molecular Formula | C44H44F6N6O10S2 |
| Exact Mass | 994.246453 g/mol |
| Enantiomer InChIKey | DROUKDWQTHEUBY-COQWMNJGSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CD3OD |
8,10-bis(chloranyl)-6a-(trifluoromethyl)-12H-[1,3]benzoxazino[3,2-a][3,1]benzoxazin-5-one
7-Amino-5-(2-chlorophenyl)-1,3-dimethyl-2,4-dioxo-1,3,4,5-tetrahydro-2H-pyrano[2,3-d]pyrimidine-6-carbonitrile
DI-[6-METHYL-8-ALPHA-(DIETHYLCARBAMOYLAMINO)-ERGOLINE-1-YL]-METHANE
(20R,22E)-24-NORCHOLESTA-5,22-DIENE-2-BETA,3-ALPHA,21-TRIOL-3,21-DISULFATE
CYTOCHALASIN_Z_12
(9E)-3-(4-chlorophenyl)-9-(4-fluorobenzylidene)-5-(4-fluorophenyl)-6,7,8,9-tetrahydro-5H-[1,3]thiazolo[2,3-b]quinazoline
9,10-DIHYDRO-YOHIMBINE
(2,7-di-tert-butyl-9H-fluoren-9-yl)(prop-1-en-2-yloxy)bis(2,4,6-tri-tert-butylphenyl)stannane
Spiro[2-oxo-1,2,3,4-tetrahydro-1-azaphenanthrene-3,2'-hexahydropyrano[2,3-b]-1-azaphenanthrrene]
4H-Pyrano[2, 3-d]pyrimidine-3-carbonitrile, 5,6,7,8-tetrahydro-2-amino-4-(2-fluorophenyl)-6,8-dimethyl-5,7-dioxo-
| Title | Journal or Book | Year |
|---|---|---|
| Synthesis of skeletally diverse alkaloid-like molecules: exploitation of metathesis substrates assembled from triplets of building blocks | Beilstein Journal of Organic Chemistry | 2013 |