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5-Indolealdehyde

Basic information

  • Product Name:5-Indolealdehyde
  • CAS No.:1196-69-6
  • EINECS No.:627-955-1
  • MF:C9H7NO

Product Specifications

  • Appearance:Off-white or light-yellow crystalline powder
  • Specification:98.5%
  • Package:1/5/10/25kgs/drum
  • Supply Capacity:Tons
  • UN number:-
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Product Details

CAS No:1196-69-6

MF:C9H7NO

Appearance:Off-white or light-yellow crystalline powder

Specification:98.5%

UN number:-

Package:1/5/10/25kgs/drum

Supply Capacity:Tons

Synonyms:1H-indol-5-carbaldehyde;1H-INDOLE-5-CARBALDEHYDE;1H-INDOLE-5-CARBOXALDEHYDE;5-INDOLE ALDEHYDE;5-FORMYLINDOLE;INDOLE-5-CARBALDEHYDE;INDOLE-5-ALDEHYDE;INDOLE-5-CARBOXALDEHYDE,Indole-5-carboxaldehyde,"Indole-5-carboxaldehyde; 1196-69-6; DTXSID20343325; DTXCID80294405; 627-955-1; 1H-Indole-5-carbaldehyde; 5-Formylindole; 1h-indole-5-carboxaldehyde; MFCD02093664; indole-5-carbaldehyde; Indole-5-aldehyde; CHEMBL3358223; 5-formyl-indole; 5-Formyl indole; Indole-5-carboaldehyde; indole 5-carboxaldehyde; Indole-5-carboxaldehyde (5-Formylindole); 1H-indol-5-carbaldehyde; SCHEMBL97207; SCHEMBL97208; 5-INDOLECARBOXALDEHYDE; 1H-Indole-5-carbaldehyde #; Indole-5-carboxaldehyde, 98%; SCHEMBL3927657; SCHEMBL31341461; ADZUEEUKBYCSEY-UHFFFAOYSA-; ALBB-004800; BCP27554; CS-D1053; BDBM50037782; SBB047518; STK501456; AKOS000121181; AB10798; FF16209; PS-3327; NCGC00188180-01; NCGC00188180-02; AC-27774; SY014625; DB-031771; I0674; ST50823968; EN300-28247; AB01320191-02; F0001-0322; Z254198328; InChI=1/C9H7NO/c11-6-7-1-2-9-8(5-7)3-4-10-9/h1-6,10H",145.160,C9H7NO,


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5-Indolealdehyde (CAS 1196-69-6), also known as Indole-5-carboxaldehyde, serves as a vital heterocyclic building block in pharmaceutical R&D and advanced fine chemical synthesis. Benefiting from the highly reactive formyl group at the 5-position of the indole ring, it is extensively utilized in the preparation of biologically active molecules, including antiproliferative, anti-inflammatory agents (curcumin derivatives), Aurora kinase A inhibitors, and topoisomerase I inhibitors. Additionally, it plays an important role in stereoselective chemical synthesis, material science for constructing azacrown ethers, and developing diagnostic probes for β-amyloid imaging.