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[ CAS No. 932744-62-2 ] {[proInfo.proName]}

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Chemical Structure| 932744-62-2
Chemical Structure| 932744-62-2
Structure of 932744-62-2 * Storage: {[proInfo.prStorage]}
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Product Details of [ 932744-62-2 ]

CAS No. :932744-62-2 MDL No. :
Formula : C56H65ClN12O10 Boiling Point : -
Linear Structure Formula :- InChI Key :-
M.W : 1101.64 Pubchem ID :-
Synonyms :
Chemical Name :(S)-1-(Chloromethyl)-3-(5-(4-((S)-2-((S)-2-((2-(4-(2,5-dioxo-2,5-dihydro-1H-pyrrol-1-yl)butanamido)ethyl)amino)-3-methylbutanamido)-5-ureidopentanamido)benzamido)-1H-indole-2-carbonyl)-2,3-dihydro-1H-benzo[e]indol-5-yl 4-methylpiperazine-1-carboxylate

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Application In Synthesis of [ 932744-62-2 ]

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 932744-62-2 ]

[ 932744-62-2 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 1037797-29-7 ]
  • [ 80307-12-6 ]
  • [ 932744-62-2 ]
YieldReaction ConditionsOperation in experiment
51% With N-ethyl-N,N-diisopropylamine; In dichloromethane; N,N-dimethyl-formamide; at 20℃; for 2h; Compound 29: To a solution of 27 (31 mg, 0.033 mmol) in 20% DMF in dichloromethane (1 mL) were added diisopropylethylamine (22 muL, 0.13 mmol) and N-succinimidyl-4-maleimidobutyrate (14 mg, 0.049 mmol) at room temperature. The mixture thus obtained was stirred for 2 hours. The solvent was evaporated and the residue was purified by semi-preparative HPLC to give compound 29 as a white solid (32 mg, 51%). 1H NMR (CD3OD) delta 1.09 (d, 3H), 1.15 (d, 3H), 1.62 (m, 2H), 1.84 (m, 1H), 1.92 (m, 3H), 2.25 (m, 3H), 2.97 (s, 3H), 3.12-3.25 (m, 6H), 3.39-3.68 (m, 10H), 3.85 (d, 1H), 3.93 (dd, 1H), 4.08 (m, 1H), 4.50-4.67 (m, 4H), 6.80 (s, 2H), 7.03 (s, 1H), 7.34 (m, 2H), 7.44 (m, 1H), 7.50 (m, 1H), 7.72 (d, 2H), 7.77 (d, 1H), 7.90 (m, 3H), 8.04 (s, 1H), 8.25 (bs, 1H); LC-MS (ES+) 552 (M+2H/2)+.
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