27421-51-8

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27421-51-8 Structure

Identification	Back 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 Properties	Back 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 Data	Back 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

[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 Detail	Back Directory
[Spectrum Detail] 1-METHYLINDOLE-2-CARBOXALDEHYDE 97(27421-51-8)IR

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