4-Aminoindole

Modify Date: 2024-01-01 19:35:40

4-Aminoindole Structure
4-Aminoindole structure
Common Name 4-Aminoindole
CAS Number 5192-23-4 Molecular Weight 132.163
Density 1.3±0.1 g/cm3 Boiling Point 354.0±15.0 °C at 760 mmHg
Molecular Formula C8H8N2 Melting Point 106-109 °C(lit.)
MSDS Chinese USA Flash Point 195.0±7.6 °C
Symbol GHS07
GHS07
Signal Word Warning

 Names

Name 1H-indol-4-amine
Synonym More Synonyms

 Chemical & Physical Properties

Density 1.3±0.1 g/cm3
Boiling Point 354.0±15.0 °C at 760 mmHg
Melting Point 106-109 °C(lit.)
Molecular Formula C8H8N2
Molecular Weight 132.163
Flash Point 195.0±7.6 °C
Exact Mass 132.068741
PSA 41.81000
LogP 0.86
Vapour Pressure 0.0±0.8 mmHg at 25°C
Index of Refraction 1.758
Storage condition −20°C
Water Solubility Insoluble

 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-S24/25
RIDADR NONH for all modes of transport
WGK Germany 3
HS Code 29339990

 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%

 Articles4

More Articles
Synthesis and in vitro and in vivo antitumor activity of 2-phenylpyrroloquinolin-4-ones.

J. Med. Chem. 48(9) , 3417-27, (2005)

In our search for potential new anticancer drugs, we designed and synthesized a series of tricyclic compounds containing the antimitotic 2-phenylazaflavone chromophore fused to a pyrrole ring in a pyr...

Cytokinin activity of azaindene, azanaphthalene, naphthalene, and indole derivatives. Torigoe Y, et al.

Phytochemistry 11(5) , 1623-1630, (1972)

Synthestic approaches to the teleocidin-related tumour promoters: a total synthesis of (±)-indolactam V. de Laszlo SE, et al.

J. Chem. Soc. Chem. Commun. 4 , 344-346., (1986)

 Synonyms

1H-Indol-4-ylamine
4-Aminoindole
4-Indolamine
indole-4-ylamine
(Indol-4-yl)amine
4-amino-1h-indole
MFCD01076559
6-amino-1H-indole
1h-indol-4-amin
1H-indole-4-amine
1H-Indol-4-amine
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