Indole-4-carboxaldehyde

Basic information

  • Product Name:Indole-4-carboxaldehyde
  • CAS No.:1074-86-8
  • EINECS No.:625-162-5
  • MF:C9H7NO

Product Specifications

  • Appearance: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:1074-86-8

MF:C9H7NO

Appearance:white or light-yellow crystalline powder

Specification:98.5%

UN number:-

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

Supply Capacity:Tons

Synonyms:1H-indol-4-carbaldehyde;1H-indole-4-carbaldehyde(SALTDATA: FREE);INDOLE-4-CARBALDEHYDE;INDOLE-4-CARBOXALDEHYDE;INDOLE-4-ALDEHYDE;4-INDOLE-CARBOXALDEHYDE;Indole-4-carboxaldehyde 97%;4-Formyl-1H-indole,Indole-4-carboxaldehyde,"Indole-4-carboxaldehyde; 1074-86-8; 1H-Indole-4-carbaldehyde; indole-4-carbaldehyde; CHEBI:143235; DTXSID40318838; DTXCID30269961; 625-162-5; JFDDFGLNZWNJTK-UHFFFAOYSA-N; 4-Formylindole; 1H-Indole-4-carboxaldehyde; MFCD01632221; 4-Indole-carboxaldehyde; 4-Formyl-1H-indole; 4-Indolecarbaldehyde; INDOLE-4-ALDEHYDE; NSC 337264; 4-formyl-indole; 1H-indol-4-carbaldehyde; 4-formylindol; 4-indolealdehyde; 4-formyl indole; NSC337264; 4-indolcarboxaldehyde; indol-4-carboaldehyde; indole 4carboxaldehyde; indol 4-carboxaldehyde; indole 4-carboxaldehyde; Indole-4-carboxaldehyde (4-Formylindole); 1H-indole-4-carbaldehyd; SCHEMBL97760; SCHEMBL97761; 1H-Indole-4-carbaldehyde #; Indole-4-carboxaldehyde, 97%; orb1984117; 1H- Indole- 4- carboxaldehyde; BDBM628210; HMS3650A21; ALBB-004801; SBB014557; STK292737; AKOS000265263; AB09519; BS-3817; CS-W001288; FI40250; HY-W001288; NSC-337264; NCGC00329124-01; AC-23426; PD020355; SY013097; DB-031770; DB-340277; ST4140235; I0712; NS00015304; EN300-66992; AB01323273-02; SR-01000946761; SR-01000946761-1; Z1065768492",145.160,C9H7NO,


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Indole-4-carboxaldehyde is primarily used as a vital pharmaceutical intermediate and an organic synthesis building block. It serves as a key precursor in the synthesis of Aurora kinase A inhibitors, E. coli cell division inhibitors, and various anti-tumor and anti-viral targeted therapeutics. Additionally, it is widely utilized as a reactant in the Biginelli reaction and intramolecular Friedel-Crafts acylation to construct complex nitrogen-containing heterocyclic alkaloids, Schiff bases, and advanced functional materials in fine chemical industries.