5,11-Dihydroindolo[3,2-b]carbazole - ≥98%(HPLC) , CAS No.6336-32-9

CAS: 6336-32-9 Cat. No.: D154424 Molecular Weight: 256.31 EC Number: 833-804-2

GRADE & PURITY ≥98%(HPLC)

Synonyms

Indolo(3,2-b)carbazole, 6,12-dihydro- | DTXSID40979504 | 5,11-Dihydridoindolo[3,2-b]carbazole | SCHEMBL550602 | 10.14272/YCPBCVTUBBBNJJ-UHFFFAOYSA-N.1 | AKOS025117422 | Indolo[3,2-b]carbazole, 5,11-dihydro- | NSC39037 | NSC-39037 | doi:10.14272/YCPBCVTUBB

Storage

Room temperature

Shipped In

Normal

Specifications

Synonyms

Indolo(3, 2-b)carbazole, 6, 12-dihydro- | DTXSID40979504 | 5, 11-Dihydridoindolo[3, 2-b]carbazole | SCHEMBL550602 | 10.14272/YCPBCVTUBBBNJJ-UHFFFAOYSA-N.1 | AKOS025117422 | Indolo[3, 2-b]carbazole, 5, 11-dihydro- | NSC39037 | NSC-39037 | doi:10.14272/YCPBCVTUBB

Specifications & Purity

≥98%(HPLC)

Storage

Room temperature

Shipped In

Normal

Purity

≥98%(HPLC)

Names and Identifiers

• Pubchem Sid: 488186947
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/488186947
• Canonical Smiles: C1=CC=C2C(=C1)C3=CC4=C(C=C3N2)C5=CC=CC=C5N4
• IUPAC Name: 5,11-dihydroindolo[3,2-b]carbazole
• InChIKey: YCPBCVTUBBBNJJ-UHFFFAOYSA-N
• INCHI: 1S/C18H12N2/c1-3-7-15-11(5-1)13-9-18-14(10-17(13)19-15)12-6-2-4-8-16(12)20-18/h1-10,19-20H
• Isomeric SMILES: C1=CC=C2C(=C1)C3=CC4=C(C=C3N2)C5=CC=CC=C5N4
• Molecular Weight: 256.31
• Reaxy-Rn: 616585
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=616585&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organoheterocyclic compounds
    • Class Indoles and derivatives
      • Subclass Carbazoles
        • Level5 Pyrrolocarbazoles
          • Level6 Indolocarbazoles

• Kingdom: Organic compounds
• Superclass: Organoheterocyclic compounds
• Class: Indoles and derivatives
• Subclass: Carbazoles
• Intermediate Tree Nodes: Pyrrolocarbazoles
• Direct Parent: Indolocarbazoles
• Alternative Parents: Indoles Benzenoids Pyrroles Heteroaromatic compounds Azacyclic compounds Organopnictogen compounds Organonitrogen compounds Hydrocarbon derivatives
• Molecular Framework: Aromatic heteropolycyclic compounds
• Substituents: Indolocarbazole - Indole - Benzenoid - Heteroaromatic compound - Pyrrole - Azacycle - Organic nitrogen compound - Organopnictogen compound - Hydrocarbon derivative - Organonitrogen compound - Aromatic heteropolycyclic compound
• Description: This compound belongs to the class of organic compounds known as indolocarbazoles. These are polycyclic aromatic compounds containing an indole fused to a carbazole.
• External Descriptors: Not available

Data sources

1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.

DOI: 10.1186/s13321-016-0174-y

Associated Targets(Human)

AHR Tclin Aryl hydrocarbon receptor (1071 Activities)

Discover Target: AHR

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Mechanisms of Action

Chemical and Physical Properties

• Melt Point(°C): 460 °C
• Molecular Weight: 256.300 g/mol
• XLogP3: 5.200
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 0
• Rotatable Bond Count: 0
• Exact Mass: 256.1 Da
• Monoisotopic Mass: 256.1 Da
• Topological Polar Surface Area: 31.600 Ų
• Heavy Atom Count: 20
• Formal Charge: 0
• Complexity: 346.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 0
• Undefined Atom Stereocenter Count: 0
• Defined Bond Stereocenter Count: 0
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 0
• Covalently-Bonded Unit Count: 1

References

1. Wang Yuting, Tan Khai Chen, Wen Hong, Zhou Panwang, Yu Yang, Guo Jiaquan, Sun Jinglu, Fang Chong, Guo Xin, Guo Jingwei, He Teng, Chen Ping.  (2026)  Alkali metal N-heteroarenes as a new family of luminescent materials.  Nature Communications,      [PMID:] [10.1038/s41467-026-72600-8]