Basic information Safety Supplier Related

1H-INDOLE-6-METHANAMINE

Basic information Safety Supplier Related

1H-INDOLE-6-METHANAMINE Basic information

Product Name:
1H-INDOLE-6-METHANAMINE
Synonyms:
  • RARECHEM AL BW 2435
  • 1-(1H-indol-6-yl)methanamine
  • (1H-indol-6-ylmethyl)amine(SALTDATA: FREE)
  • INDOLE-6-METHYLAMINE
  • 1H-INDOLE-6-METHANAMINE
  • 6-(Aminomethyl)indole
  • 1H-Indol-6-ylmethylamine
  • (1H-Indol-6-yl)methanamine
CAS:
3468-17-5
MF:
C9H10N2
MW:
146.19
Product Categories:
  • Building Blocks
  • C7 to C10
  • C7 to C9
  • Chemical Synthesis
  • Halogenated Heterocycles
  • Heterocyclic Building Blocks
  • Indoles
  • New Products for Chemical Synthesis
Mol File:
3468-17-5.mol
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1H-INDOLE-6-METHANAMINE Chemical Properties

Melting point:
135-140℃
Boiling point:
335.6±17.0 °C(Predicted)
Density 
1.199±0.06 g/cm3(Predicted)
storage temp. 
under inert gas (nitrogen or Argon) at 2–8 °C
form 
solid
pka
17.21±0.30(Predicted)
Appearance
Off-white to light yellow Solid
Water Solubility 
Slightly soluble in water.
Sensitive 
Moisture Sensitive
CAS DataBase Reference
3468-17-5
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Safety Information

Hazard Codes 
Xi,Xn
Risk Statements 
22-37/38-41
Safety Statements 
26-39
WGK Germany 
3
HazardClass 
IRRITANT
HS Code 
2933998090
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1H-INDOLE-6-METHANAMINE Usage And Synthesis

Uses

6-(Aminomethyl)indole is used as an organic chemical synthesis intermediate.

Synthesis

15861-36-6

3468-17-5

Example 71 Preparation of 1H-indole-6-methylamine: 1H-indole-6-carbonitrile (prepared by literature methods: Batcho, AD; Leimgruber, W. Organic Syntheses 1985, 63, 214-225; 1.50 g, 10.6 mmol) was hydrogenated overnight at atmospheric pressure over a nickel Nguyenne catalyst in a mixture of ethanol (50 mL) and concentrated ammonia (4 mL). (4 mL) in a mixed solution of ethanol (50 mL) and concentrated ammonia (4 mL) at atmospheric pressure overnight for hydrogenation. Upon completion of the reaction, the reaction mixture was filtered through Celite to remove the catalyst. The filter cake was washed well with ethanol, taking care to avoid drying of the catalyst. The filtrates were combined and concentrated to afford 1H-indole-6-methylamine (1.50 g, 97% yield).

References

[1] Patent: US2002/161237, 2002, A1

1H-INDOLE-6-METHANAMINESupplier

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