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

3 Citations COA COA
    Grade & Purity:
  • ≥98%
In stock
Item Number
P101988
Grouped product items
SKU Size
Availability
 Price Qty
P101988-1g
1g
≥10
$10.90
P101988-5g
5g
Available within 4-8 weeks(?)
Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!
$27.90
P101988-25g
25g
2
$135.90
P101988-100g
100g
1
$489.90
P101988-500g
500g
Available within 4-8 weeks(?)
Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!
$2,200.90
Wish List
Bulk Order  SDS  DATASHEET  Specification Sheet
View related series
azole (525) Five-Membered Heterocyclic Compounds (2064)

Basic Description

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 Temp Argon charged
Shipped In Normal
Product Description

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.

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
Superclass Organoheterocyclic compounds
Class Indoles and derivatives
Subclass Carbazoles
Intermediate Tree Nodes Not available
Direct Parent Carbazoles
Alternative Parents Phenylpyrroles  Indoles  Benzene and substituted derivatives  Heteroaromatic compounds  Azacyclic compounds  Organopnictogen compounds  Organonitrogen compounds  Hydrocarbon derivatives  
Molecular Framework Aromatic 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
Description 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 Not available

Associated Targets(Human)

GLP1R Tclin Glucagon-like peptide 1 receptor (111429 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
ATM Tchem Serine-protein kinase ATM (4198 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
KDM4A Tchem Lysine-specific demethylase 4A (52245 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
TDP1 Tchem Tyrosyl-DNA phosphodiesterase 1 (345557 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
L3MBTL1 Tchem Lethal(3)malignant brain tumor-like protein 1 (14536 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
KDM4E Tchem Lysine-specific demethylase 4D-like (40243 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
GMNN Tbio Geminin (128009 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
CBX1 Tbio Chromobox protein homolog 1 (92434 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
BAZ2B Tchem Bromodomain adjacent to zinc finger domain protein 2B (56204 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
USP1 Tchem Ubiquitin carboxyl-terminal hydrolase 1 (22556 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID

Associated Targets(non-human)

Streptococcus (3973 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Pseudomonas aeruginosa (123386 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Klebsiella pneumoniae (43867 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Staphylococcus aureus (210822 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Acinetobacter baumannii (41033 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Escherichia coli (133304 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Plasmodium falciparum (966862 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Cryptococcus neoformans (21258 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Candida albicans (78123 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Streptococcus sp. 'group A' (3417 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
HT-22 (3261 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
ska Streptokinase A (5805 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID

Mechanisms of Action

Mechanism of Action Action Type target ID Target Name Target Type Target Organism Binding Site Name References

Names and Identifiers

Pubchem Sid 488184611
Pubchem Sid Url https://pubchem.ncbi.nlm.nih.gov/substance/488184611
IUPAC Name 9-phenylcarbazole
INCHI InChI=1S/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
InChIKey VIJYEGDOKCKUOL-UHFFFAOYSA-N
Smiles C1=CC=C(C=C1)N2C3=CC=CC=C3C4=CC=CC=C42
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=

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.

17 results found

Lot Number Certificate Type Date Item
D2116389 Certificate of Analysis Jan 09, 2025 P101988
G2415787 Certificate of Analysis Apr 29, 2024 P101988
G2415792 Certificate of Analysis Apr 29, 2024 P101988
G2415793 Certificate of Analysis Apr 29, 2024 P101988
L1903068 Certificate of Analysis Sep 12, 2023 P101988
H2322715 Certificate of Analysis Jul 31, 2023 P101988
H2322652 Certificate of Analysis Jul 31, 2023 P101988
H2322653 Certificate of Analysis Jul 31, 2023 P101988
K2420084 Certificate of Analysis Jul 31, 2023 P101988
H2322655 Certificate of Analysis Jul 31, 2023 P101988
H2322651 Certificate of Analysis Jul 31, 2023 P101988
H2322654 Certificate of Analysis Jul 31, 2023 P101988
E23161128 Certificate of Analysis May 20, 2023 P101988
I1514057 Certificate of Analysis May 08, 2023 P101988
B2311343 Certificate of Analysis Feb 18, 2023 P101988
A2305097 Certificate of Analysis Jan 09, 2023 P101988
K2222357 Certificate of Analysis Nov 30, 2022 P101988

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Chemical and Physical Properties

Solubility Slightly soluble in water.
Sensitivity Air sensitive
Melt Point(°C) 95-97°C
Molecular Weight 243.300 g/mol
XLogP3 5.000
Hydrogen Bond Donor Count 0
Hydrogen Bond Acceptor Count 0
Rotatable Bond Count 1
Exact Mass 243.105 Da
Monoisotopic Mass 243.105 Da
Topological Polar Surface Area 4.900 Ų
Heavy Atom Count 19
Formal Charge 0
Complexity 285.000
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

Citations of This Product

How to Cite Aladdin Scientific Products?
1. Jian Wang, Congcong Wang, Hongchao Wang, Bo Jin, Peiping Zhang, Lina Li, Shiding Miao.  (2021)  Synthesis of N-containing porous aromatic frameworks via Scholl reaction for reversible iodine capture.  MICROPOROUS AND MESOPOROUS MATERIALS,  310  (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,    (1-16). 
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,  502  (158017). 

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