ChemicalBook--->CAS DataBase List--->24621-70-3

24621-70-3

24621-70-3 Structure

24621-70-3 Structure
IdentificationBack Directory
[Name]

1H-INDOL-2-YLMETHANOL
[CAS]

24621-70-3
[Synonyms]

NSC 165230
1H-Indole-2-methanol
indol-2-ylmethan-1-ol
1H-INDOL-2-YLMETHANOL
2-HYDROXYMETHYLINDOLE
1H-Indole-2-methanol 90%
2-(Hydroxymethyl)-1H-indole
2-(Hydroxymethyl)-1H-indole 97+%
[Molecular Formula]

C9H9NO
[MDL Number]

MFCD00030195
[MOL File]

24621-70-3.mol
[Molecular Weight]

147.17
Chemical PropertiesBack Directory
[Melting point ]

72-78 °C
[Boiling point ]

360.6±17.0 °C(Predicted)
[density ]

1.272±0.06 g/cm3(Predicted)
[storage temp. ]

Keep in dark place,Inert atmosphere,2-8°C
[form ]

solid
[pka]

14.86±0.10(Predicted)
[Appearance]

Light brown to yellow Solid
[InChI]

InChI=1S/C9H9NO/c11-6-8-5-7-3-1-2-4-9(7)10-8/h1-5,10-11H,6H2
[InChIKey]

XEEANGGQJOWRTG-UHFFFAOYSA-N
[SMILES]

N1C2=C(C=CC=C2)C=C1CO
Safety DataBack Directory
[Symbol(GHS) ]

GHS hazard pictograms
GHS05
[Signal word ]

Danger
[Hazard statements ]

H318
[Precautionary statements ]

P280-P305+P351+P338
[Hazard Codes ]

Xi
[Risk Statements ]

41
[Safety Statements ]

26
[WGK Germany ]

3
[HS Code ]

2933998090
[Storage Class]

11 - Combustible Solids
[Hazard Classifications]

Eye Dam. 1
Hazard InformationBack Directory
[Uses]

Reactant for the synthesis of:
  • Oxazino[4,3-a]indoles
  • 2-arylsulfonylmethyl-3-piperazinylmethylindole derivatives as 5-HT6 receptor ligands
  • SR13668 designed to mimic the unique anticancer mechanisms of dietary indole-3-carbinol to block Akt signaling
  • Azido- and isothiocyanato-substituted indoles as melatoninergic agents
[Synthesis]

Put 20kg of 4-oxoindole, 4kg of Pd/C catalyst with 5% Pd content (palladium carbon catalyst) and 60L of diethylene glycol dimethyl ether as solvent into a 100L reactor with stirring device, and then heat up the reactor with steam, turn on the stirring, an
Spectrum DetailBack Directory
[Spectrum Detail]

1H-INDOL-2-YLMETHANOL(24621-70-3)1HNMR
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