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1-Acetyl-3-indolecarboxaldehyde_Molecular_structure_CAS_22948-94-3)
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1-Acetyl-3-indolecarboxaldehyde

Catalog No. 375772 Name Sigma Aldrich
CAS Number 22948-94-3 Website http://www.sigmaaldrich.com
M. F. C11H9NO2 Telephone 1-800-521-8956
M. W. 187.19466 Fax
Purity 98% Email
Storage Chembase ID: 91254

SYNONYMS

Title
N-乙酰基吲哚-3-甲醛
IUPAC name
1-acetyl-1H-indole-3-carbaldehyde
IUPAC Traditional name
1-acetylindole-3-carbaldehyde
Synonyms
N-Acetylindol-3-carboxaldehyde
NSC 61289

DATABASE IDS

EC Number 245-347-0
CAS Number 22948-94-3
MDL Number MFCD00039691
PubChem SID 24863403

PROPERTIES

Empirical Formula (Hill Notation) C11H9NO2
Purity 98%
Melting Point 165 °C(lit.)
GHS Pictograms GHS07
GHS Signal Word Warning
GHS Hazard statements H315-H319-H335
European Hazard Symbols Irritant Irritant (Xi)
MSDS Link Download
Personal Protective Equipment dust mask type N95 (US), Eyeshields, Gloves
GHS Precautionary statements P261-P305 + P351 + P338
Risk Statements 36/37/38
Safety Statements 26-36
German water hazard class 3

DETAILS

Description (English)
Packaging
5 g in glass bottle
Application
Reactant for synthesis of α-ketoamides as inhibitors of Dengue virus protease with antiviral activity in cell-culture1Reactant for preparation of homoallylic amines as antimicrobial agents2Reactant for preparation of pyrrole-based hydrazones as potential tuberculostatics3Reactant for synthesis of neoechinulin A and derivatives4Reactant for synthesis of substituted (Z)-2-(N-benzylindol-3-ylmethylene)quinuclidin-3-one and (Z)-(±)-2-(N-benzylindol-3-ylmethylene)quinuclidin-3-ol derivatives as potent thermal sensitizing agents5Reactant for preparation of RNA-specific live cell imaging probes E36, E144 and F226
Description (简体中文)
包装
5 g in glass bottle
Application
Reactant for synthesis of α-ketoamides as inhibitors of Dengue virus protease with antiviral activity in cell-culture1Reactant for preparation of homoallylic amines as antimicrobial agents2Reactant for preparation of pyrrole-based hydrazones as potential tuberculostatics3Reactant for synthesis of neoechinulin A and derivatives4Reactant for synthesis of substituted (Z)-2-(N-benzylindol-3-ylmethylene)quinuclidin-3-one and (Z)-(±)-2-(N-benzylindol-3-ylmethylene)quinuclidin-3-ol derivatives as potent thermal sensitizing agents5Reactant for preparation of RNA-specific live cell imaging probes E36, E144 and F226

REFERENCES