Name: Carbazole - ≥96% , CAS No.86-74-8
Brand: Aladdin Scientific
SKU: C104875
Availability: InStock

Carbazole - ≥96% , CAS No.86-74-8

CAS: 86-74-8 Cat. No.: C104875 Summenformel: C₁₂H₉N Molekulargewicht: 167.21 Beilstein Registry Number: 3956 EG-Nummer: 201-696-0

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QUALITÄT & REINHEIT ≥96%

Synonyms

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Übersicht Spezifikationen Namen und Kennungen Dokumentation Erweiterte Daten Taxonomic Classification 3D-Struktur Zugehörige Ziele (menschlich) Zugehörige Ziele (nicht menschlich) Wirkungsmechanismen Zertifikate (CoA, COO, BSE/TSE und Analyse-Diagramm) Chemische und physikalische Eigenschaften FAQs und Artikel Citations of This Product Lösungsrechner Bewertungen

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Warum diese Qualität

≥96% für empfindliche chromatographische und analytische Workflows, die minimale Basislinieninterferenzen erfordern.

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Lagerung & Versand

Room temperature Versand FedEx DG Service. Genaue Spezifikationen finden Sie im chargenspezifischen COA.

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Qualitätsdokumente

SDS, COA, Datenblatt und Spezifikationsblatt stehen zum Download bereit. Chargenspezifische COA über Chargennummernsuche abrufbar.

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Literaturbeleg

In 71 peer-reviewten Publikationen zu Chromatographie, organischer Synthese und Kreuzkupplungsreaktionen zitiert.

Übersicht

Carbazole is an aromatic heterocyclic organic molecule. It mainly interacts with DNA and damages it. These events suppress the synthesis of new DNA or RNA. Carbazole derivatives are involved in antimicrobial, antitumor, antiepileptic, antihistaminic, antioxidant, anti-inflammatory, antidiarrhoeal, analgesic, neuroprotective and pancreatic lipase suppression activities.
Carbazole has been used in the uronic acid assay

Spezifikationen

Synonyme

Spezifikationen & Reinheit

≥96%

Storage

Room temperature

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Reinheit

≥96%

Namen und Kennungen

Pubchem Sid

488180177

Pubchem Sid Url

https://pubchem.ncbi.nlm.nih.gov/substance/488180177

Kanonisches Lächeln

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

IUPAC Name

9H-carbazole

InChIKey

UJOBWOGCFQCDNV-UHFFFAOYSA-N

INCHI

1S/C12H9N/c1-3-7-11-9(5-1)10-6-2-4-8-12(10)13-11/h1-8,13H

Isomere SMILES

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

WGK Deutschland

RTECS

FE3150000

UN-Nummer

3077

Verpackungsgruppe

III

Molekulargewicht

167.21

Beilstein

3956

Reaxy-Rn

3956

Reaxys-RN_link_address

https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=3956&ln=

Dokumentation

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Erweiterte Daten

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
- Superclass Organoheterocyclic compounds
  - Klasse Indoles and derivatives
    - Subclass Carbazoles

Kingdom	Organic compounds
Superclass	Organoheterocyclic compounds
Klasse	Indoles and derivatives
Subclass	Carbazoles
Intermediate Tree Nodes	Not available
Direct Parent	Carbazoles
Alternative Parents	Indoles Benzenoids Pyrroles Heteroaromatic compounds Azacyclic compounds Organopnictogen compounds Organonitrogen compounds Hydrocarbon derivatives
Molecular Framework	Aromatic heteropolycyclic compounds
Substituents	Carbazole - Indole - Benzenoid - Heteroaromatic compound - Pyrrole - Azacycle - Organic nitrogen compound - Organopnictogen compound - Hydrocarbon derivative - Organonitrogen compound - Aromatic heteropolycyclic compound
Beschreibung	This compound belongs to the class of organic compounds known as carbazoles. These are compounds containing a three ring system containing a pyrrole ring fused on either side to a benzene ring.
External Descriptors	a carbazole
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

3D-Struktur

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AR Tclin Androgen Receptor (11781 Activities)

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

TYR Tclin Tyrosinase (717 Activities)

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PTH1R Tclin Parathyroid hormone receptor (47172 Activities)

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ALDH1A1 Tchem Aldehyde dehydrogenase 1A1 (77053 Activities)

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U-937 (7138 Activities)

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KIF11 Tchem Kinesin-like protein 1 (1720 Activities)

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HSD17B10 Tchem Endoplasmic reticulum-associated amyloid beta-peptide-binding protein (20669 Activities)

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Staphylococcus aureus (210822 Activities)

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Bovine viral diarrhea virus 1 (1277 Activities)

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Nfe2l2 Nuclear factor erythroid 2-related factor 2 (214 Activities)

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Rorc Nuclear receptor ROR-gamma (89407 Activities)

Discover Target: Rorc

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

clpP ATP-dependent Clp protease proteolytic subunit (245 Activities)

Discover Target: clpP

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

Wirkungsmechanismen

Zertifikate (CoA, COO, BSE/TSE und Analyse-Diagramm)

C of A & Other Certificates(BSE/TSE, COO):

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27 results found

Lot Number	Certificate Type	Datum	Artikel
E2626330	Certificate of Analysis	Jun 06, 2026	C104875
E2626328	Certificate of Analysis	Jun 06, 2026	C104875
E2626321	Certificate of Analysis	Jun 06, 2026	C104875
F2528101	Certificate of Analysis	Jul 05, 2025	C104875
F2530069	Certificate of Analysis	Jul 02, 2025	C104875
F2530068	Certificate of Analysis	Jul 02, 2025	C104875
F2530006	Certificate of Analysis	Jul 02, 2025	C104875
D2621034	Certificate of Analysis	Jul 02, 2025	C104875
B2505091	Certificate of Analysis	Feb 08, 2025	C104875
D2115186	Certificate of Analysis	Jan 10, 2025	C104875
D2115188	Certificate of Analysis	Jan 10, 2025	C104875
D2115182	Certificate of Analysis	Jan 10, 2025	C104875
H2322042	Certificate of Analysis	Aug 25, 2023	C104875
B2306864	Certificate of Analysis	Feb 09, 2023	C104875
C23201125	Certificate of Analysis	Sep 17, 2022	C104875
F23051075	Certificate of Analysis	Sep 17, 2022	C104875
I2214366	Certificate of Analysis	Sep 17, 2022	C104875
I2214367	Certificate of Analysis	Sep 17, 2022	C104875
I2214368	Certificate of Analysis	Sep 17, 2022	C104875
I2214369	Certificate of Analysis	Sep 17, 2022	C104875
L2404065	Certificate of Analysis	Jan 21, 2022	C104875
B2306861	Certificate of Analysis	Jan 21, 2022	C104875
A2212198	Certificate of Analysis	Jan 21, 2022	C104875
A2212195	Certificate of Analysis	Jan 21, 2022	C104875
A2212194	Certificate of Analysis	Jan 21, 2022	C104875
A2212193	Certificate of Analysis	Jan 18, 2022	C104875
A2418042	Certificate of Analysis	Apr 22, 2021	C104875

Chemische und physikalische Eigenschaften

Löslichkeit	It is insoluble in water;Solubility in hot EtOH:almost transparency
Flammpunkt (°F)	428℉
Flammpunkt (°C)	220°C
Siedepunkt (°C)	355°C
Schmelzpunkt (°C)	245°C
Molekulargewicht	167.210 g/mol
XLogP3	3.700
Hydrogen Bond Donor Count	1
Hydrogen Bond Acceptor Count	0
Rotatable Bond Count	0
Exact Mass	167.073 Da
Monoisotopic Mass	167.073 Da
Topological Polar Surface Area	15.800 Å²
Heavy Atom Count	13
Formal Charge	0
Complexity	170.000
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

FAQs und Artikel

Light-Emitting Polymers (LEPs): A Practical Panorama - A Core PL/EL Mechanistic Framework, Material Family Map, and Structural “Design Knobs” (including Product Tables 1–4 and a selection guide)

Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides

Tags:

Light-Emitting Polymers LEPs

Why Carbazole Is So Common in OLEDs: Managing Charge Carriers, Excitons, and Film Morphology with a Building-Block Mindset (with Selection Guide and Tables 1–3)

Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides

Tags:

OLED

Pyrrole Research Reagent Selection Roadmap: Structure—Reactive Sites—Application Throughline and Reagent Classification Guide (Tables 1–4)

Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides

Tags:

Pyrrole five-membered aromatic

Citations of This Product

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📚 Zitationen nach Anwendung

Extraction & workup solvent21

Organic synthesis — reaction medium42

Polymer synthesis & polymerization10

Other applications33

Electrochemistry & battery electrolyte12

Spectroscopy sample preparation3

Chromatography (HPLC / GC / TLC)5

Cross-coupling reactions1

Controlled-release & nanoparticle carrier1

Topical & ophthalmic formulation1

Drug / compound screening1

Industrial & non-pharma application1

Crystallization & recrystallization2

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Carbazole - ≥96% , CAS No.86-74-8

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