Indole-5-carboxaldehyde

Modify Date: 2024-01-02 10:00:46

Indole-5-carboxaldehyde Structure
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
GHS07
Signal Word Warning

 Names

Name Indole-5-carboxaldehyde
Synonym More Synonyms

 Chemical & Physical Properties

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

 Safety Information

Symbol GHS07
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

 Synthetic Route

 Customs

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%

 Articles14

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Synthesis and antifungal activity of novel streptochlorin analogues.

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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...

 Synonyms

MFCD02093664
5-Formylindole
1H-Indole-5-carboxaldehyde
Indole-5-carboxaldehyde
1H-Indole-5-carbaldehyde
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