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1-Acetyl-1H-indole-3-carbaldehyde

Base Information
  • Chemical Name:1-Acetyl-1H-indole-3-carbaldehyde
  • CAS No.:22948-94-3
  • Molecular Formula:C11H9NO2
  • Molecular Weight:187.198
  • Hs Code.:29339990
  • European Community (EC) Number:245-347-0
  • NSC Number:61289
  • UNII:56ESZ895CE
  • DSSTox Substance ID:DTXSID60177489
  • Nikkaji Number:J307.765I
  • Wikidata:Q72435301
  • Metabolomics Workbench ID:123890
  • ChEMBL ID:CHEMBL1650260
  • Mol file:22948-94-3.mol
1-Acetyl-1H-indole-3-carbaldehyde

Synonyms:22948-94-3;1-Acetyl-1H-indole-3-carbaldehyde;N-Acetylindole-3-carboxaldehyde;1-Acetyl-3-indolecarboxaldehyde;1-acetylindole-3-carbaldehyde;1-Acetylindole-3-carboxaldehyde;1H-Indole-3-carboxaldehyde, 1-acetyl-;56ESZ895CE;EINECS 245-347-0;1-Acetyl-1H-indole-3-carboxaldehyde;MFCD00039691;NSC-61289;1-acetyl-3-formylindole;NSC61289;OpticalBrightenerVBL;N-acetylindole-3-aldehyde;UNII-56ESZ895CE;SCHEMBL870631;N-Acetylindol-3-carboxaldehyde;CHEMBL1650260;DTXSID60177489;CHEBI:133207;BCP26459;NSC 61289;STK386919;AKOS001588414;1-Acetyl-3-indolecarboxaldehyde, 98%;N-ACETYL-3-INDOLECARBOXALDEHYDE;PS-5825;NCGC00186378-01;SY061794;INDOLE-3-CARBOXALDEHYDE, 1-ACETYL-;CS-0142077;FT-0607280;A-1400

Suppliers and Price of 1-Acetyl-1H-indole-3-carbaldehyde
Supply Marketing:
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
  • TRC
  • 1-Acetyl-1H-indole-3-carbaldehyde
  • 2.5g
  • $ 75.00
  • SynQuest Laboratories
  • 1-Acetyl-1H-indole-3-carboxaldehyde
  • 1 g
  • $ 16.00
  • SynQuest Laboratories
  • 1-Acetyl-1H-indole-3-carboxaldehyde
  • 5 g
  • $ 34.00
  • SynQuest Laboratories
  • 1-Acetyl-1H-indole-3-carboxaldehyde
  • 25 g
  • $ 136.00
  • Sigma-Aldrich
  • 1-Acetyl-3-indolecarboxaldehyde 98%
  • 5g
  • $ 55.10
  • Matrix Scientific
  • 1-Acetyl-1H-indole-3-carbaldehyde
  • 25g
  • $ 118.00
  • Matrix Scientific
  • 1-Acetyl-1H-indole-3-carbaldehyde
  • 5g
  • $ 28.00
  • Frontier Specialty Chemicals
  • N-Acetyl-3-indolecarboxaldehyde 98%
  • 1g
  • $ 18.00
  • Frontier Specialty Chemicals
  • N-Acetyl-3-indolecarboxaldehyde 98%
  • 5g
  • $ 61.00
  • Crysdot
  • 1-Acetyl-1H-indole-3-carbaldehyde 97%
  • 100g
  • $ 303.00
Total 76 raw suppliers
Chemical Property of 1-Acetyl-1H-indole-3-carbaldehyde
Chemical Property:
  • Appearance/Colour:Light yellow crystals 
  • Vapor Pressure:0.000116mmHg at 25°C 
  • Melting Point:165 °C(lit.) 
  • Refractive Index:1.598 
  • Boiling Point:336 °C at 760 mmHg 
  • Flash Point:157 °C 
  • PSA:39.07000 
  • Density:1.19 g/cm3 
  • LogP:2.11390 
  • Storage Temp.:2-8°C 
  • Sensitive.:Air Sensitive 
  • XLogP3:1.3
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:2
  • Rotatable Bond Count:1
  • Exact Mass:187.063328530
  • Heavy Atom Count:14
  • Complexity:252
Purity/Quality:

99% *data from raw suppliers

1-Acetyl-1H-indole-3-carbaldehyde *data from reagent suppliers

Safty Information:
  • Pictogram(s): IrritantXi 
  • Hazard Codes:Xi 
  • Statements: 36/37/38 
  • Safety Statements: 26-36 
MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:
  • Canonical SMILES:CC(=O)N1C=C(C2=CC=CC=C21)C=O
  • Uses Reactant for synthesis of α-ketoamides as inhibitors of Dengue virus protease with antiviral activity in cell-cultureReactant for preparation of homoallylic amines as antimicrobial agentsReactant for preparation of pyrrole-based hydrazones as potential tuberculostaticsReactant for synthesis of neoechinulin A and derivativesReactant 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 agentsReactant for preparation of RNA-specific live cell imaging probes E36, E144 and F22
Technology Process of 1-Acetyl-1H-indole-3-carbaldehyde

There total 9 articles about 1-Acetyl-1H-indole-3-carbaldehyde which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:
Guidance literature:
With sodium hydroxide; tetra(n-butyl)ammonium hydrogensulfate; In dichloromethane; Heating;
Guidance literature:
With dmap; triethylamine; In dichloromethane; at 0 - 20 ℃; for 3h; Inert atmosphere;
DOI:10.1021/acs.orglett.1c01134
Guidance literature:
With Iron(III) nitrate nonahydrate; 2,2,6,6-Tetramethyl-1-piperidinyloxy free radical; oxygen; sodium chloride; In 1,2-dichloro-ethane; at 20 ℃; for 1.5h;
DOI:10.1039/c3ob40226f
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