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

CAS: 1150-62-5 Cat. No.: P101988 Molecular Weight: 243.3 Beilstein Registry Number: 20(1)164 EC Number: 214-564-2
AVAILABLE TO ORDER
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
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Size
Status
Price
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1g
P101988-1g
≥10
$9.90
5g
P101988-5g
1
$10.90
25g
P101988-25g
2

$15.90

$23.90
Save $8.00 (33.47%)
100g
P101988-100g
1

$62.90

$94.90
Save $32.00 (33.72%)
500g
P101988-500g
8-12 wks(?) Production requires sourcing of materials. We appreciate your patience and understanding.

$263.90

$395.90
Save $132.00 (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.

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Quality documents

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

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Literature proof

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

Overview

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

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
Specifications & Purity
≥98%
Storage
Argon charged, Room temperature
Shipped In
Normal
Purity
≥98%
Names and Identifiers
Pubchem Sid488184611
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/488184611
Canonical SmilesC1=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
Isomeric SMILES C1=CC=C(C=C1)N2C3=CC=CC=C3C4=CC=CC=C42
WGK Germany 3
Molecular Weight 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
ClassIndoles 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
DescriptionThis 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
3D Structure
Interactive Chemical Structure Model





Associated Targets(Human)
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
Associated Targets(non-human)
Streptococcus (3973 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Pseudomonas aeruginosa (123386 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Klebsiella pneumoniae (43867 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Staphylococcus aureus (210822 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
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)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Cryptococcus neoformans (21258 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Candida albicans (78123 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Streptococcus sp. 'group A' (3417 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HT-22 (3261 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ska Streptokinase A (5805 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mechanisms of Action
Certificates(CoA,COO,BSE/TSE and Analysis Chart)
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 TypeDateItem
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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Chemical and Physical Properties
SolubilitySlightly soluble in water.
SensitivityAir sensitive
Melt Point(°C)95-97°C
Molecular Weight243.300 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
Documents & Articles
Citations of This Product
References
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]
Solution Calculators
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