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Sigma Aldrich 5,7-Dichloro-1H-indole-2-carboxylic acid
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Description
- 3-butyn-2-one undergoes asymmetric double-michael reaction with ortho-tosylamidophenyl malonate catalyzed by chiral aminophosphines to yield indolines
- It undergoes double michael reaction with nitrogen-containing tethered diacid to give pipecolic acid derivatives.3-butyn-2-one was used in the synthesis of clerodane diterpenoid (+/-)-sacacarin
- It was used as substrate in stereoselective, conjugate arylation mediated by gallium(iii) chloride leading to (e)-α,α-unsaturated ketones
Specifications
Specifications
| Molecular Formula | C9H5Cl2NO2 |
| Linear Formula | C9H5Cl2NO2 |
| MDL Number | MFCD02664420 |
| Quantity | 2.5 mL |
| Molecular Weight (g/mol) | 230.05 |
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