6H-Indolo(2,3-b)quinoxaline

Basic Information

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CAS Number

84055-81-2

Molecular Formula

C14H9N3

Molecular Weight

219.25 g/mol

Chemical Classification

Basic Chemical Raw Materials Organic Chemicals Heterocyclic Compounds

Pharmaceutical Chemicals Pharmaceutical Intermediates Heterocyclic Intermediates

Basic Physical Properties

SMILES

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C1=CC=C2C(=C1)C3=NC4=CC=CC=C4N=C3N2

InChI

InChI=1S/C14H9N3/c1-2-6-10-9(5-1)13-14(16-10)17-12-8-4-3-7-11(12)15-13/h1-8H,(H,16,17)

InChIKey

LCKIWLDOHFUYDV-UHFFFAOYSA-N

LogP

3.2643000000000013

Topological Polar Surface Area

41.57 Å²

Hydrogen Bond Donor/Acceptor

1 / 3

Complexity

293

Synonyms & References

English

6H-Indolo[2,3-b]quinoxaline
SMR000068993
indolo[2,3-b]quinoxaline
243-61-8
SR-01000554124
SCHEMBL278729
MLS000053030
6H-Indolo(2,3-b)quinoxaline
HMS623H13
SR-01000554124-1
BDBM42826
Z57102758
SCHEMBL17693674
F1394-0001
6H-indolo[3,2-b]quinoxaline
CBDivE_001230
cid_5356192
5H-Indolo[2,3-b]quinoxaline
AKOS005749491
DB-219850
243-59-4
ChemDiv1_012839
Oprea1_859350
AIDS124803
LS-04323
Oprea1_264584
NSC 52574
NSC52574
DTXSID401309710
STL149578
MFCD00068754

MDL Number

MFCD00068754

FAQ

What are the physical and chemical properties of 6H-Indolo(2,3-b)quinoxaline (CAS: 84055-81-2)?

6H-Indolo(2,3-b)quinoxaline is a crystalline solid with a molecular weight of approximately 256.24 g/mol. It has a high solubility in organic solvents such as DMF and DMSO but is less soluble in water. The compound is known for its moderate reactivity, particularly in nucleophilic substitution reactions.

How is 6H-Indolo(2,3-b)quinoxaline (CAS: 84055-81-2) typically synthesized?

6H-Indolo(2,3-b)quinoxaline is typically synthesized via a multistep process involving the condensation of indole with quinoxaline derivatives. Common methods include using piperidine or morpholine as the condensing agent under basic conditions. The process yields approximately 70-80% product purity with good selectivity.

What industries use 6H-Indolo(2,3-b)quinoxaline (CAS: 84055-81-2)?

6H-Indolo(2,3-b)quinoxaline is used in pharmaceuticals for its potential as an antiviral agent, in polymers for its thermal stability, in sensors for its sensing capabilities, and in semiconductors for its electronic properties. It is also explored in research for its biological activity.

What precautions should be taken when handling 6H-Indolo(2,3-b)quinoxaline (CAS: 84055-81-2)?

Proper handling of 6H-Indolo(2,3-b)quinoxaline requires the use of appropriate personal protective equipment (PPE), including gloves, goggles, and a lab coat. Ensure the use of a fume hood during operations to minimize inhalation risk. In case of a spill, thoroughly clean up according to standard procedures and refer to the safety data sheet (SDS) for further guidance.