Indole-5-carboxaldehyde structure
|
Common Name | Indole-5-carboxaldehyde | ||
---|---|---|---|---|
CAS Number | 1196-69-6 | Molecular Weight | 145.158 | |
Density | 1.3±0.1 g/cm3 | Boiling Point | 339.1±15.0 °C at 760 mmHg | |
Molecular Formula | C9H7NO | Melting Point | 100-103 °C(lit.) | |
MSDS | Chinese USA | Flash Point | 166.8±27.8 °C | |
Symbol |
GHS07 |
Signal Word | Warning |
Name | Indole-5-carboxaldehyde |
---|---|
Synonym | More Synonyms |
Density | 1.3±0.1 g/cm3 |
---|---|
Boiling Point | 339.1±15.0 °C at 760 mmHg |
Melting Point | 100-103 °C(lit.) |
Molecular Formula | C9H7NO |
Molecular Weight | 145.158 |
Flash Point | 166.8±27.8 °C |
Exact Mass | 145.052765 |
PSA | 32.86000 |
LogP | 1.56 |
Vapour Pressure | 0.0±0.7 mmHg at 25°C |
Index of Refraction | 1.729 |
Storage condition | Keep Cold |
Symbol |
GHS07 |
---|---|
Signal Word | Warning |
Hazard Statements | H315-H319-H335 |
Precautionary Statements | P261-P305 + P351 + P338 |
Personal Protective Equipment | dust mask type N95 (US);Eyeshields;Gloves |
Hazard Codes | Xi:Irritant |
Risk Phrases | R36/37/38 |
Safety Phrases | S26-S36/37/39 |
RIDADR | NONH for all modes of transport |
WGK Germany | 3 |
HS Code | 2933990090 |
Precursor 8 | |
---|---|
DownStream 10 | |
HS Code | 2933990090 |
---|---|
Summary | 2933990090. heterocyclic compounds with nitrogen hetero-atom(s) only. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0% |
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. Bas... |
|
Synthesis and antiproliferative activity of novel 2-aryl-4-benzoyl-imidazole derivatives targeting tubulin polymerization.
Bioorg. Med. Chem. 19 , 4782-95, (2011) We previously reported the discovery of 2-aryl-4-benzoyl-imidazoles (ABI-I) as potent antiproliferative agents for melanoma. To further understand the structural requirements for the potency of ABI an... |
|
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 titani... |
MFCD02093664 |
5-Formylindole |
1H-Indole-5-carboxaldehyde |
Indole-5-carboxaldehyde |
1H-Indole-5-carbaldehyde |