#21;(R,R,R)-2-(3-[6-[5-(N-TERT.-BUTOXYCARBONYL-2-METHOXYCARBONYL-METHYLAMINO)-3-IODO-2-METHOXYPHENYL]-INDOL-3-YL]-2-CARBOBENZYLOXYAMINOPROPIONYLAMINO)-2-(3,5-D
Compound with spectra: 1 NMR
![#21;(R,R,R)-2-(3-[6-[5-(N-TERT.-BUTOXYCARBONYL-2-METHOXYCARBONYL-METHYLAMINO)-3-IODO-2-METHOXYPHENYL]-INDOL-3-YL]-2-CARBOBENZYLOXYAMINOPROPIONYLAMINO)-2-(3,5-D](/api/compound/2TMhVcV7uZi.png?ph=true&h=300&w=458 "#21;(R,R,R)-2-(3-[6-[5-(N-TERT.-BUTOXYCARBONYL-2-METHOXYCARBONYL-METHYLAMINO)-3-IODO-2-METHOXYPHENYL]-INDOL-3-YL]-2-CARBOBENZYLOXYAMINOPROPIONYLAMINO)-2-(3,5-D")
| SpectraBase Compound ID | 2TMhVcV7uZi |
|---|---|
| InChI | InChI=1S/2C47H51Cl2IN4O11/c2*1-46(2,3)64-43(57)37(27-19-32(48)40(61-8)33(49)20-27)53-41(55)35(52-44(58)63-24-25-14-11-10-12-15-25)22-28-23-51-38-29(28)16-13-17-30(38)31-18-26(21-34(50)39(31)60-7)36(42(56)62-9)54-45(59)65-47(4,5)6/h2*10-21,23,35-37,51H,22,24H2,1-9H3,(H,52,58)(H,53,55)(H,54,59)/t2*35-,36+,37-/m00/s1 |
| InChIKey | JETVEETYHXXLMQ-ZODVCHPOSA-N |
| Mol Weight | 2091.5 g/mol |
| Molecular Formula | C94H102Cl4I2N8O22 |
| Exact Mass | 2088.395218 g/mol |
| Enantiomer InChIKey | JETVEETYHXXLMQ-UZOBTFIBSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
#22;(R,R,R)-2-[3-(3-[N-[2-(3,5-DICHLORO-4-METHOXYPHENYL)-ACETYLCARBOXYL]-2-CARBOBENZYLOXYAMINOPROPIONYLAMINO]-INDOL-7-YL)-5-IODO-4-METHOXYPHENYL]-2-METHOXYCARB
10-Phenylcarbonyl-4-(4'-phenylcarbonylphenyl)-1-n-octyl-1H-phenanthro [9,10-d]-1,2,3-triazole
(2S,5S)-2-(4-methoxyphenyl)-5-phenyl-3-pyrroline-2,3,4-tricarboxylic acid trimethyl ester
2-(N-BUTYL)-5-METHOXY-7-PHENYL-2H-BENZO-[DE]-ISOQUINOLINE-1,6-DIONE
CBZ-rhazinal
3-quinolinecarboxylic acid, 4-(2-chloro-5-nitrophenyl)-1,4,5,6,7,8-hexahydro-2,7,7-trimethyl-5-oxo-, (4-methoxyphenyl)methyl ester
N-Ethyl-Laurolitsine
1'-Benzylspiro[1,3,4-benzotriazepine-2,3'-indole]-2',5(1H,1'H)-dione
LAUREN-1-EN-14-ONE
3-(1-(furan-2-ylmethyl)-5-methoxy-2-methyl-1H-indol-3-yl)-4-phenyl-1H-1,2,4-triazole-5(4H)-thione
| Title | Journal or Book | Year |
|---|---|---|
| Preparation of 7-Halo-indoles by Thallation of N-Formylindoline and Their Attempted Use for Synthesis of the Right-Hand Segment of Chloropeptin | Chemical and Pharmaceutical Bulletin | 2006 |