9-Phenylcarbazole - ≥98% , CAS No.1150-62-5

CAS: 1150-62-5 Cat. No.: P101988 Peso molecular: 243.3 Beilstein Registry Number: 20(1)164 Número EC: 214-564-2
Disponible para pedir
GRADE & PURITY ≥98%
Synonyms
Carbazole, 9-phenyl- | DTXSID50150928 | InChI=1/C18H13N/c1-2-8-14(9-3-1)19-17-12-6-4-10-15(17)16-11-5-7-13-18(16)19/h1-13 | 1,7-Heptanedicarboxylic acid | 9-phenyl carbazole | AC-22292 | cid_70851 | P1492 | 1H-INDOLE-3-CARBOXYLICACIDBENZYLAMIDE | NCGC0024
Storage
Argon charged,Room temperature
Shipped In
Normal
 ·  off list, applied to all prices below.
Size
Estado
Price
Qty
1g
P101988-1g
≥10
9,90US$
5g
P101988-5g
1
10,90US$
25g
P101988-25g
2

15,90US$

23,90US$
Guardar 8,00 US$ (33.47%)
100g
P101988-100g
1

62,90US$

94,90US$
Guardar 32,00 US$ (33.72%)
500g
P101988-500g
8-12 wks(?) Production requires sourcing of materials. We appreciate your patience and understanding.

263,90US$

395,90US$
Guardar 132,00 US$ (33.34%)
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Why this grade

≥98% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Argon charged,Room temperature Ships Normal Check lot-specific COA for exact specifications.

📋

Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

📚

Literature proof

Cited in 3 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Descripción general

Application

9-Phenylcarbazole has been used in the electrochemical synthesis of poly(9-phenylcarbazole) films via direct anodic oxidation in mixed electrolytes of boron trifluoride diethyl etherate and sulfuric acid.

Specifications

Sinónimos
Carbazole, 9-phenyl- | DTXSID50150928 | InChI=1/C18H13N/c1-2-8-14(9-3-1)19-17-12-6-4-10-15(17)16-11-5-7-13-18(16)19/h1-13 | 1, 7-Heptanedicarboxylic acid | 9-phenyl carbazole | AC-22292 | cid_70851 | P1492 | 1H-INDOLE-3-CARBOXYLICACIDBENZYLAMIDE | NCGC0024
Especificaciones y pureza
≥98%
Condiciones de almacenamiento de almacenamiento
Argon charged, Room temperature
Enviado en
Normal
Pureza
≥98%
Nombres e identificadores
Pubchem Sid488184611
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/488184611
Sonrisas canónicasC1=CC=C(C=C1)N2C3=CC=CC=C3C4=CC=CC=C42
IUPAC Name9-phenylcarbazole
InChIKeyVIJYEGDOKCKUOL-UHFFFAOYSA-N
INCHI1S/C18H13N/c1-2-8-14(9-3-1)19-17-12-6-4-10-15(17)16-11-5-7-13-18(16)19/h1-13H
Isómeros SMILES C1=CC=C(C=C1)N2C3=CC=CC=C3C4=CC=CC=C42
WGK Alemania 3
Peso molecular 243.3
Beilstein 20(1)164
Reaxy-Rn 169982
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=169982&ln=

Documentation

📋 Safety Data Sheet (SDS)

Comprehensive hazard, handling, storage, and regulatory compliance document.

Download SDS →

✅ Certificate of Analysis (COA)

Lot-specific quality data. Enter your lot number to retrieve the exact COA.

Look up COA →

📊 Datasheet

Quick-reference summary of product specifications and applications.

View datasheet →

🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

View spec sheet →

Advanced Data

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassOrganoheterocyclic compounds
ClaseIndoles and derivatives
SubclassCarbazoles
Intermediate Tree Nodes Not available
Direct ParentCarbazoles
Alternative Parents Phenylpyrroles  Indoles  Benzene and substituted derivatives  Heteroaromatic compounds  Azacyclic compounds  Organopnictogen compounds  Organonitrogen compounds  Hydrocarbon derivatives  
Molecular FrameworkAromatic heteropolycyclic compounds
Substituents Carbazole - 1-phenylpyrrole - Indole - Benzenoid - Substituted pyrrole - Monocyclic benzene moiety - Heteroaromatic compound - Pyrrole - Azacycle - Organic nitrogen compound - Organopnictogen compound - Hydrocarbon derivative - Organonitrogen compound - Aromatic heteropolycyclic compound
DescripciónThis 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 Not available
Estructura 3D
Modelo de Estructura Química Interactiva





Objetivos asociados (humanos)
GLP1R Tclin Glucagon-like peptide 1 receptor (111429 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ATM Tchem Serine-protein kinase ATM (4198 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
KDM4A Tchem Lysine-specific demethylase 4A (52245 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
TDP1 Tchem Tyrosyl-DNA phosphodiesterase 1 (345557 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
L3MBTL1 Tchem Lethal(3)malignant brain tumor-like protein 1 (14536 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
KDM4E Tchem Lysine-specific demethylase 4D-like (40243 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
GMNN Tbio Geminin (128009 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CBX1 Tbio Chromobox protein homolog 1 (92434 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
BAZ2B Tchem Bromodomain adjacent to zinc finger domain protein 2B (56204 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
USP1 Tchem Ubiquitin carboxyl-terminal hydrolase 1 (22556 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Objetivos asociados (no humanos)
Streptococcus (3973 Activities)
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Pseudomonas aeruginosa (123386 Activities)
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Klebsiella pneumoniae (43867 Activities)
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Staphylococcus aureus (210822 Activities)
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Acinetobacter baumannii (41033 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Escherichia coli (133304 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Plasmodium falciparum (966862 Activities)
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Cryptococcus neoformans (21258 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Candida albicans (78123 Activities)
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Streptococcus sp. 'group A' (3417 Activities)
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HT-22 (3261 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ska Streptokinase A (5805 Activities)
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Mecanismos de acción
Certificados (CoA, COO, BSE/TSE y tabla de análisis)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

19 results found

Lot NumberCertificate TypeFechaArticulo
D2116389Certificate of AnalysisJan 09, 2025 P101988
G2415787Certificate of AnalysisApr 29, 2024 P101988
G2415792Certificate of AnalysisApr 29, 2024 P101988
G2415793Certificate of AnalysisApr 29, 2024 P101988
L1903068Certificate of AnalysisSep 12, 2023 P101988
H2322651Certificate of AnalysisJul 31, 2023 P101988
K2420084Certificate of AnalysisJul 31, 2023 P101988
H2322715Certificate of AnalysisJul 31, 2023 P101988
H2322655Certificate of AnalysisJul 31, 2023 P101988
H2322654Certificate of AnalysisJul 31, 2023 P101988
H2322653Certificate of AnalysisJul 31, 2023 P101988
H2322652Certificate of AnalysisJul 31, 2023 P101988
G2509057Certificate of AnalysisJul 31, 2023 P101988
E2619039Certificate of AnalysisJul 31, 2023 P101988
E23161128Certificate of AnalysisMay 20, 2023 P101988
I1514057Certificate of AnalysisMay 08, 2023 P101988
B2311343Certificate of AnalysisFeb 18, 2023 P101988
A2305097Certificate of AnalysisJan 09, 2023 P101988
K2222357Certificate of AnalysisNov 30, 2022 P101988

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Propiedades químicas y físicas
SolubilidadSlightly soluble in water.
SensibilidadAir sensitive
Punto de fusión (°C)95-97°C
Peso molecular243.300 g/mol
XLogP35.000
Hydrogen Bond Donor Count0
Hydrogen Bond Acceptor Count0
Rotatable Bond Count1
Exact Mass243.105 Da
Monoisotopic Mass243.105 Da
Topological Polar Surface Area4.900 Ų
Heavy Atom Count19
Formal Charge0
Complexity285.000
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count1
Preguntas frecuentes y artículos
Citations of This Product
Referencias
1. Jian Wang, Congcong Wang, Hongchao Wang, Bo Jin, Peiping Zhang, Lina Li, Shiding Miao.  (2020)  Synthesis of N-containing porous aromatic frameworks via Scholl reaction for reversible iodine capture.  MICROPOROUS AND MESOPOROUS MATERIALS,      [PMID:] [10.1016/j.micromeso.2020.110596]
2. Wang Yifan, Dong Wenjian, Yan Xuefeng, Li Xia, Yu Liangmin.  (2025)  Synthesis and antifouling properties of carbazole amide derivatives with fluorescent functional structure.  JOURNAL OF MATERIALS SCIENCE,      [PMID:] [10.1007/s10853-025-10725-9]
3. Wenjian Dong, Yifan Wang, Xia Li, Liangmin Yu, Na Li, Jian Yang, Junchao Yin.  (2024)  Synthesis and marine antifouling properties of carbazole amide derivatives with fluorescent properties and their zinc acrylate resins.  CHEMICAL ENGINEERING JOURNAL,      [PMID:] [10.1016/j.cej.2024.158017]
Calculadoras de soluciones
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