1H-Indole-4-carbaldehyde
1H-Indole-4-carbaldehyde structure
|
Common Name | 1H-Indole-4-carbaldehyde | ||
|---|---|---|---|---|
| CAS Number | 1074-86-8 | Molecular Weight | 145.16 | |
| Density | 1.3±0.1 g/cm3 | Boiling Point | 339.1±15.0 °C at 760 mmHg | |
| Molecular Formula | C9H7NO | Melting Point | 139-143 °C(lit.) | |
| MSDS | Chinese USA | Flash Point | 166.8±27.8 °C | |
| Symbol |
GHS07 |
Signal Word | Warning | |
|
One-pot synthesis of 2-substituted indoles from 2-aminobenzyl phosphonium salts. A formal total synthesis of arcyriacyanin A.
Org. Lett. 10(14) , 3061-3, (2008) The reaction of (2-aminobenzyl) triphenylphosphonium bromide with aromatic aldehydes or alpha,beta-unsaturated aldehydes under microwave-assisted conditions constitutes a new synthesis of 2-substituted indoles in high yields (81-97%) in a one-pot reaction. Th... |
|
|
Synthesis and biological evaluation of achiral indole-substituted titanocene dichloride derivatives.
Int J Med Chem 2012 , 905981, (2015) Six new titanocene compounds have been isolated and characterised. These compounds were synthesised from their fulvene precursors using Super Hydride (LiBEt3H) followed by transmetallation with titanium tetrachloride to yield the corresponding titanocene dich... |
|
|
A New Synthesis method of indole-4-carboxaldehyde. Wu Y-M, et al.
Chinese J. Synth. Chem. 12 , 333-35, (2004)
|
|
|
Total syntheses of clavine alkaloids by an intramolecular nitrone-olefin cycloaddition reaction. Oppolzer W, et al.
Tetrahedron 39(22) , 3695-3705, (1983)
|
|
|
Synthesis of (-)-chanoclavine I. Kardos N and Genet J-P.
Tetrahedron Asymmetry 5(8) , 1525-33, (1994)
|
|
|
Synthesis of Fused 4, 5-Disubstituted Indole Ring Systems by Intramolecular Friedel-Crafts Acylation of 4-Substituted Indoles. Fillion E and Dumas AM.
J. Org. Chem. 73(7) , 2920-23, (2008)
|