| Identification | Back Directory | [Name]
(S)-TERT-BUTYL 1-(CHLOROMETHYL)-5-HYDROXY-1H-BENZO[E]INDOLE-3(2H)-CARBOXYLATE | [CAS]
130007-86-2 | [Synonyms]
N-Boc-seco-CBI
(S)-TERT-BUTYL 1-(CHLOROMETHYL)-5-HYDROXY-1H-BENZO[E]INDOLE-3(2H)-CARBOXYLATE
tert-Butyl (S)-1-(chloromethyl)-5-hydroxy-1,2-dihydro-3H-benzo[e]indole-3-carboxylate
(S)-tert-Butyl 1-(chloromethyl)-5-hydroxy-1H-benzo[e]indole-3(2H)-carboxylate 95% (HPLC)
3H-Benz[e]indole-3-carboxylic acid, 1-(chloromethyl)-1,2-dihydro-5-hydroxy-, 1,1-dimethylethyl ester, (1S)- | [Molecular Formula]
C18H20ClNO3 | [MDL Number]
MFCD29059844 | [MOL File]
130007-86-2.mol | [Molecular Weight]
333.81 |
| Chemical Properties | Back Directory | [Melting point ]
161 °C (decomp) | [Boiling point ]
493.7±45.0 °C(Predicted) | [density ]
1.275±0.06 g/cm3(Predicted) | [storage temp. ]
-20°C | [form ]
powder | [pka]
9.63±0.40(Predicted) | [optical activity]
[α]/D -89.0, c = 0.05% in chloroform |
| Hazard Information | Back Directory | [Uses]
N-Boc-CBI best used as its seco precursor (seco-N-Boc-CBI) is a simple alkylation subunit analog of that found in the naturally occurring antitumor agents the duocarmycins, yatakemycin, and CC-1065, which act by sequence selective DNA alkylation. |
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