alpha-carboline
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
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
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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