ChemicalBook--->CAS DataBase List--->15861-36-6

15861-36-6

15861-36-6 Structure

15861-36-6 Structure
IdentificationMore
[Name]

6-Cyanoindole
[CAS]

15861-36-6
[Synonyms]

6-CYANOINDOLE
CYANOINDOLE-6
INDOLE-6-CARBONITRILE
1H-indole-6-carbonitrile
6-Cyanoidole
Indole-6-carbonitrile, 98+%
6-Indolecarbonitrile
6-Cyano-1H-indole
[EINECS(EC#)]

239-988-5
[Molecular Formula]

C9H6N2
[MDL Number]

MFCD00016732
[Molecular Weight]

142.16
[MOL File]

15861-36-6.mol
Chemical PropertiesBack Directory
[Appearance]

Off-White Crystalline Solid
[Melting point ]

130-132°C
[Boiling point ]

350.0±15.0 °C(Predicted)
[density ]

1.24±0.1 g/cm3(Predicted)
[storage temp. ]

Keep in dark place,Inert atmosphere,Room temperature
[solubility ]

Dichloromethane, Methanol
[form ]

Solid
[pka]

15.17±0.30(Predicted)
[color ]

Off-White Crystalline
[Sensitive ]

Air & Light Sensitive
[BRN ]

116502
[InChI]

InChI=1S/C9H6N2/c10-6-7-1-2-8-3-4-11-9(8)5-7/h1-5,11H
[InChIKey]

SZSZDBFJCQKTRG-UHFFFAOYSA-N
[SMILES]

N1C2=C(C=CC(C#N)=C2)C=C1
[CAS DataBase Reference]

15861-36-6(CAS DataBase Reference)
Safety DataBack Directory
[Symbol(GHS) ]

Skull and Crossbones (GHS06)Exclamation Mark (GHS07)
GHS06,GHS07
[Signal word ]

Danger
[Hazard statements ]

H302-H335-H301-H315-H319
[Precautionary statements ]

P261-P280a-P304+P340-P305+P351+P338-P501a-P264-P270-P280-P301+P310+P330-P302+P352+P332+P313+P362+P364-P305+P351+P338+P337+P313-P405-P501
[Hazard Codes ]

Xi
[Risk Statements ]

R22:Harmful if swallowed.
[Safety Statements ]

S22:Do not breathe dust .
S36/37:Wear suitable protective clothing and gloves .
[RIDADR ]

3439
[HazardClass ]

6.1
[PackingGroup ]

III
[HS Code ]

29339900
Hazard InformationBack Directory
[Chemical Properties]

Off-White Crystalline Solid
[Uses]

6-Cyanoindole (cas# 15861-36-6) is a compound useful in organic synthesis.
[Synthesis]

4-Methyl-3-nitrobenzonitrile

939-79-7

Acetic acid

64-19-7

6-Cyanoindole

15861-36-6

To a stirred solution of 4-methyl-3-nitrobenzonitrile (16.58 g, 102.3 mmol) in 55 mL of N,N-dimethylformamide (DMF) was added N,N-dimethylacetamide (15.24 g, 128.1 mmol). The reaction mixture turned dark red and was subsequently stirred at 110 °C for 3 hours. After completion of the reaction, the solvent was removed under reduced pressure and the residue was dissolved in a mixture of 300 mL of ethanol and 300 mL of acetic acid. The reaction mixture was heated to 60 °C and iron powder (33 g, 594 mmol) was added in batches. The reaction mixture was refluxed for 2 h. After the reaction was completed, it was filtered through a Hyflo pad. Ether was added to the filtrate and the acidic layer was extracted with ether (1×). The ether layers were combined and concentrated in vacuum. The residue was purified by silica gel column chromatography using dichloromethane as eluent to give 7.02 g (48% yield) of 6-cyanoindaha solid.

[References]

[1] Patent: US2006/122189, 2006, A1. Location in patent: Page/Page column 20
Spectrum DetailBack Directory
[Spectrum Detail]

6-Cyanoindole(15861-36-6)MS
6-Cyanoindole(15861-36-6)1HNMR
6-Cyanoindole(15861-36-6)13CNMR
6-Cyanoindole(15861-36-6)IR1
6-Cyanoindole(15861-36-6)IR2
Well-known Reagent Company Product InformationBack Directory
[Alfa Aesar]

Indole-6-carbonitrile, 98+%(15861-36-6)
[TCI AMERICA]

6-Cyanoindole,>98.0%(GC)(15861-36-6)
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