ChemicalBook--->CAS DataBase List--->3468-17-5

3468-17-5

3468-17-5 Structure

3468-17-5 Structure
IdentificationBack Directory
[Name]

1H-INDOLE-6-METHANAMINE
[CAS]

3468-17-5
[Synonyms]

RARECHEM AL BW 2435
INDOLE-6-METHYLAMINE
6-(Aminomethyl)indole
1H-INDOLE-6-METHANAMINE
1H-Indol-6-ylmethylamine
Indole, 6-(aminomethyl)-
6-(Aminomethyl)indole 97%
(1H-Indol-6-yl)methanamine
1-(1H-indol-6-yl)methanamine
(1H-indol-6-ylmethyl)amine(SALTDATA: FREE)
[Molecular Formula]

C9H10N2
[MDL Number]

MFCD06213839
[MOL File]

3468-17-5.mol
[Molecular Weight]

146.19
Chemical PropertiesBack Directory
[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
Safety DataBack Directory
[Hazard Codes ]

Xi,Xn
[Risk Statements ]

22-37/38-41
[Safety Statements ]

26-39
[WGK Germany ]

3
[HazardClass ]

IRRITANT
[HS Code ]

2933998090
Hazard InformationBack Directory
[Uses]

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

6-Cyanoindole

15861-36-6

1H-INDOLE-6-METHANAMINE

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
Spectrum DetailBack Directory
[Spectrum Detail]

1H-INDOLE-6-METHANAMINE(3468-17-5)1HNMR
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