Basic information Safety Supplier Related

Indole-4-carboxylic acid

Basic information Safety Supplier Related

Indole-4-carboxylic acid Basic information

Product Name:
Indole-4-carboxylic acid
Synonyms:
  • INDOLE-4-CARBOXYLIC ACID
  • 1H-INDOLE-4-CARBOXYLIC ACID
  • 1H-4-INDOLECARBOXYLIC ACID
  • RARECHEM AL BE 1201
  • 4-INDOLECARBOXYLIC ACID
  • 4-CARBOXYINDOLE
  • Indole-4-Carbocylic acid
  • 4-INDOLE CARBOXYLIC ACIDINDOLE-4-CARBOXYLIC ACID
CAS:
2124-55-2
MF:
C9H7NO2
MW:
161.16
EINECS:
621-279-0
Product Categories:
  • Heterocycle-Indole series
  • Simple Indoles
  • Indole
  • Indoles
  • Building Blocks
  • Heterocyclic Building Blocks
  • blocks
  • Carboxes
  • IndolesOxindoles
  • Indole/indoline/oxindole
  • Indole and Indoline
  • Indoles and derivatives
Mol File:
2124-55-2.mol
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Indole-4-carboxylic acid Chemical Properties

Melting point:
213-214 °C (lit.)
Boiling point:
213-214℃
Density 
1.408±0.06 g/cm3(Predicted)
storage temp. 
Keep in dark place,Sealed in dry,Room Temperature
pka
3.90±0.10(Predicted)
form 
Powder
color 
Beige
InChI
InChI=1S/C9H7NO2/c11-9(12)7-2-1-3-8-6(7)4-5-10-8/h1-5,10H,(H,11,12)
InChIKey
ROGHUJUFCRFUSO-UHFFFAOYSA-N
SMILES
N1C2=C(C(C(O)=O)=CC=C2)C=C1
CAS DataBase Reference
2124-55-2(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-36
WGK Germany 
3
HazardClass 
IRRITANT
HS Code 
29339900

MSDS

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Indole-4-carboxylic acid Usage And Synthesis

Chemical Properties

Beige powder

Uses

  • Reactant for preparation of substituted indole derivatives as histamine H3 antagonists
  • Reactant for preparation of potent and selective inhibitors of human reticulocyte 15-lipoxygenase-1
  • Reactant for preparation of inhibitors of Gli1-mediated transcription in Hedgehog pathway
  • Reactant for preparation of pyridinyl carboxylates as SARS-CoV 3CL proinhibitors
  • Reactant for preparation of substituted bipiperidinylmethyl amides as CCR3 membrane binding ligands
  • Reactant for preparation of indole amide hydroxamic acids as potent inhibitors of histone deacetylases
  • Reactant for preparation of 2-[[[4′-chloro-[1,1-biphenyl]-4-yl]thio]methyl]-N-hydroxybutanamide derivatives as specific metalloproteinase

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