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27421-51-8

27421-51-8 Structure

27421-51-8 Structure
IdentificationBack Directory
[Name]

1-METHYLINDOLE-2-CARBOXALDEHYDE 97
[CAS]

27421-51-8
[Synonyms]

NSC 106285
2-Formyl-1-methylindole
2-Formyl-1-methyl-1H-indole
1-methylindole-2-carbaldehyde
1-Methyl-1H-indole-2-carbaldehyde
1H-Indole-2-carboxaldehyde,1-methy
1-METHYLINDOLE-2-CARBOXALDEHYDE 97
1-Methylindole-2-carboxaldehyde 97%
1H-Indole-2-carboxaldehyde, 1-methyl-
1H-Indole-2-carboxaldehyde, 1-methyl- (9CI)
[Molecular Formula]

C10H9NO
[MDL Number]

MFCD01863665
[MOL File]

27421-51-8.mol
[Molecular Weight]

159.185
Chemical PropertiesBack Directory
[Melting point ]

81-85 °C(lit.)
[Boiling point ]

90-95 °C(Press: 0.02 Torr)
[density ]

1.10±0.1 g/cm3(Predicted)
[storage temp. ]

under inert gas (nitrogen or Argon) at 2-8°C
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319-H335
[Precautionary statements ]

P261-P264-P271-P280-P302+P352-P305+P351+P338
[Hazard Codes ]

Xi
[Risk Statements ]

36/37/38
[Safety Statements ]

26-36
[WGK Germany ]

3
[HS Code ]

2933998090
Hazard InformationBack Directory
[Uses]

Reactant for preparation of:
  • Deazapurine isosteres from acylindoles via pyridine ring annulation
  • 2,4-dichlorocinnamohydroxamic acid analogs for enhancing pharmacokinetics of botulinum neurotoxin serotype A protease inhibitors
  • Tetrahydrocarbazoles via organocatalytic cascade Friedel-Crafts alkylation/Michael addition/aromatization reaction
  • Azides, imines and amines via flow processes of amines and trimethylsilyl azide and aza-Wittig reaction
  • 3-indolylpyridinedicarbonitriles as anti-inflammatory agents
  • Bis(indolyl)methanes as antimicrobial and antioxidant agents
Spectrum DetailBack Directory
[Spectrum Detail]

1-METHYLINDOLE-2-CARBOXALDEHYDE 97(27421-51-8)IR
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