2-Methyl-1H-indole-3-carbaldehyde
2-Methyl-1H-indole-3-carbaldehyde structure
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Common Name | 2-Methyl-1H-indole-3-carbaldehyde | ||
|---|---|---|---|---|
| CAS Number | 5416-80-8 | Molecular Weight | 159.185 | |
| Density | 1.2±0.1 g/cm3 | Boiling Point | 344.3±22.0 °C at 760 mmHg | |
| Molecular Formula | C10H9NO | Melting Point | 200-201 °C(lit.) | |
| MSDS | Chinese USA | Flash Point | 169.9±29.8 °C | |
| Symbol |
GHS07 |
Signal Word | Warning | |
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Synthesis and antifungal activity of novel streptochlorin analogues.
Eur. J. Med. Chem. 92 , 776-83, (2015) Streptochlorin, first isolated as a new antibiotic in 1988 from the lipophilic extracts of the mycelium of a Streptomyces sp, is an indole natural products with a variety of biological activities. Based on the methods developed for the synthesis of pimprinine... |
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Functionalization of benzylic C(sp(3))-H bonds of heteroaryl aldehydes through N-heterocyclic carbene organocatalysis.
Angew. Chem. Int. Ed. Engl. 52(42) , 11134-7, (2013) Aryl aldehyde activation: Oxidative activation of 2-methylindole-3-carboxaldehyde (I) through N-heterocyclic carbene (NHC) organocatalysis generates heterocyclic ortho-quinodimethane (II) as a key intermediate. This intermediate then undergoes formal [4+2] cy... |
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(2-Methyl-1-phenyl-sulfonyl-1H-indol-3-yl)methanol.
Acta Crystallogr. Sect. E Struct. Rep. Online 64(2) , o542-o542, (2008) In the title compound, C(16)H(15)NO(3)S, the plane of the phenyl ring forms a dihedral angle of 80.37 (8)° with the indole ring system. The crystal packing is stabilized by weak O-H⋯O hydrogen bonds which link the mol-ecules into infinite chains along the a a... |