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4-Aminoindole

Names

[ CAS No. ]:
5192-23-4

[ Name ]:
4-Aminoindole

[Synonym ]:
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

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

MSDS

Safety Information

[ 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-S24/25

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

[ HS Code ]:
29339990

Synthetic Route

Precursor & DownStream

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%

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)


More Articles


Related Compounds