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alpha-carboline

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alpha-carboline Basic information

Product Name:
alpha-carboline
Synonyms:
  • 1,9-Diazafluorene 1-Azacarbazole
  • 9H-1,9-Diazafluorene
  • NSC 67064
  • 1,9-Diazafluorene
  • 9H-Pyrido[2,3-b]indole
  • alpha-carboline
  • 1-Azacarbazole
  • 1H-Pyrido[2,3-b]indole
CAS:
244-76-8
MF:
C11H8N2
MW:
168.19
EINECS:
205-960-6
Product Categories:
  • Aromatics
  • Heterocycles
  • Indole Derivatives
  • Mutagenesis Research Chemicals
Mol File:
244-76-8.mol
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alpha-carboline Chemical Properties

Melting point:
210-212°C
Boiling point:
373℃
Density 
1.301
Flash point:
172℃
storage temp. 
Inert atmosphere,Room Temperature
solubility 
Acetone, DMSO, Methanol (Slightly, Hetaed)
form 
Solid
pka
14.53±0.30(Predicted)
color 
Pale Brown
λmax
338nm(CH3CN)(lit.)
InChI
InChI=1S/C11H8N2/c1-2-6-10-8(4-1)9-5-3-7-12-11(9)13-10/h1-7H,(H,12,13)
InChIKey
BPMFPOGUJAAYHL-UHFFFAOYSA-N
SMILES
N1C2=C(C=CC=C2)C2=CC=CN=C12
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Safety Information

HS Code 
2933.99.8290
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alpha-carboline Usage And Synthesis

Chemical Properties

Light Brown Solid

Uses

A carcinogenic compound formed during cooking processes

Definition

ChEBI: 9H-Pyrido[2,3-b]indole is a pyridoindole.

Synthesis

The 9H-pyrido[2,3- b]indoles were produced by dissolving 1-bromo-2-(2,2-dibromovinyl)benzene or its derivatives, ammonia and a, ??-unsaturated aldehydes in an organic solvent, and then adding a catalyst, transition metal salts and additives, and then reacting at 60-100 ??C in the presence of air. The synthesis process of the present invention is a one-pot multi-component tandem reaction, which is simple and easy to operate, and avoids the waste of resources and environmental pollution caused by the use of a variety of reagents and the purification of intermediates in each step of the reaction, and provides an economical and practical method for the synthesis of 9H-pyrido[2,3-b]indole compounds in a green and environmentally friendly way.

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