#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
Compound with spectra: 1 NMR
![#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](/api/compound/11qb9IOQnwy.png?ph=true&h=300&w=458 "#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")
| SpectraBase Compound ID | 11qb9IOQnwy |
|---|---|
| InChI | InChI=1S/2C38H35Cl2IN4O9.2C2HF3O2/c2*1-51-33-25(12-20(15-28(33)41)30(42)37(49)53-3)24-11-7-10-23-22(17-43-32(23)24)16-29(44-38(50)54-18-19-8-5-4-6-9-19)35(46)45-31(36(47)48)21-13-26(39)34(52-2)27(40)14-21;2*3-2(4,5)1(6)7/h2*4-15,17,29-31,43H,16,18,42H2,1-3H3,(H,44,50)(H,45,46)(H,47,48);2*(H,6,7)/t2*29-,30+,31-;;/m00../s1 |
| InChIKey | NSANBFVZGXAHSH-NKEITLPPSA-N |
| Mol Weight | 2007.101 g/mol |
| Molecular Formula | C80H72Cl4F6I2N8O22 |
| Exact Mass | 2004.150886 g/mol |
| Parent InChIKey | IQTNFTIQONNZGT-YPKYBTACSA-N |
| Enantiomer InChIKey | NSANBFVZGXAHSH-CUVDMYIQSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CD3OD |
#25;(R,R,R)-2-(3-[6-[5-(N-TERT.-BUTOXYCARBONYL-2-METHOXYCARBONYLMETHYLAMINO)-3-IODO-2-METHOXYPHENYL]-INDOL-3-YL]-2-CARBOBENZYLOXYAMINOPROPIONYLAMINO)-2-(3,5-DI
N-Ethyl-Laurolitsine
CBZ-rhazinal
#32B;(S,R,R)-3-[6-(5-[1-[2-(3,5-DICHLORO-4-METHOXYPHENYL)-2-TERT.-BUTOXYCARBONYLAMINO-ACETYLAMINO]-1-METHOXYCARBONYLMETHYL]-3-IODO-2-METHOXYPHENYL)-INDOL-3-YL]
#32A;(R,R,R)-3-[6-(5-[1-[2-(3,5-DICHLORO-4-METHOXYPHENYL)-2-TERT.-BUTOXYCARBONYLAMINO-ACETYLAMINO]-1-METHOXYCARBONYLMETHYL]-3-IODO-2-METHOXYPHENYL)-INDOL-3-YL]
YIFMSNBQADOPBX-UHFFFAOYSA-N
(+)-Boldine hydrochloride
1-Phenyldibenzo[j,l]fluoranthene
5-(4-ethoxyphenyl)-3-(3-methoxy-4-propoxyphenyl)-2-phenyldihydro-2H-pyrrolo[3,4-d]isoxazole-4,6(3H,5H)-dione
OSG-2;ISO-TYPE-OF-SIDE-CHAIN;MINOR
| 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 |