2-Phenylindole - ≥99% , CAS No.948-65-2

CAS: 948-65-2 Cat. No.: P111467 Summenformel: C14H11N Molekulargewicht: 193.24 Beilstein Registry Number: 20467 EG-Nummer: 213-436-3
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GRADE & PURITY ≥99%
Synonyms
EINECS 213-436-3 | MQD44HV3P1 | HMS2233J19 | NSC 15776 | SCHEMBL3835030 | SMR000526281 | DTXSID8061343 | 2-phenylindol | AB00876244-08 | alpha-Phenylindole | InChI=1/C14H11N/c1-2-6-11(7-3-1)14-10-12-8-4-5-9-13(12)15-14/h1-10,15 | SY032900 | 2-PHENYL-1H-IN
Storage
Room temperature
Shipped In
Normal
★
Size
Deutschland (EU)
USA*
Price
Qty
10g
P111467-10g
Auf Bestellung · 8–12 Wochen
8,59€
25g
P111467-25g
—
8 Auf Lager
9,46€
100g
P111467-100g
—
3 Auf Lager

13,80€

20,74€
Speichern 6,94 € (33.47%)
250g
P111467-250g
1 Auf Lager
1 Auf Lager

30,28€

45,90€
Speichern 15,62 € (34.03%)
500g
P111467-500g
1 Auf Lager
1 Auf Lager

59,79€

90,16€
Speichern 30,37 € (33.69%)
Enter a quantity for the sizes you want to add.
🧪

Why this grade

≥99% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

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 1 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Übersicht

2-Phenylindole is a reactant for preparation of organic light emitting diodes (OLEDs), anti inflammatory agents, antifungal and antibacterial agents and fluorescent probes. It is a reactant in difluorohydroxylation reactions and Mannich-type reactions.
A reactant in difluorohydroxylation reactions.


Application

Reactant for preparation of:

Oxopyrrolidine analogs via iodine-catalyzed Markovnikov addition

Tryptophan dioxygenase inhibitors pyridyl-ethenyl-indoles as potential anticancer immunomodulators

Organic light emitting diodes (OLEDs)

Anti inflammatory agents

Potential cyclooxygenase-1 (COX-1)/cyclooxygenase-2 (COX-2) inhibitors

Agents for cancer and malaria therapy

Antifungal and antibacterial agents

Fluorescent probes


Reactant in:

Difluorohydroxylation reactions†

Mannich-type reactions†

Specifications

Synonyme
EINECS 213-436-3 | MQD44HV3P1 | HMS2233J19 | NSC 15776 | SCHEMBL3835030 | SMR000526281 | DTXSID8061343 | 2-phenylindol | AB00876244-08 | alpha-Phenylindole | InChI=1/C14H11N/c1-2-6-11(7-3-1)14-10-12-8-4-5-9-13(12)15-14/h1-10,15 | SY032900 | 2-PHENYL-1H-IN
Spezifikationen & Reinheit
≥99%
Storage
Room temperature
Verschickt in
Normal
Reinheit
≥99%
Namen und Kennungen
Pubchem Sid488181891
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/488181891
Kanonisches LächelnC1=CC=C(C=C1)C2=CC3=CC=CC=C3N2
IUPAC Name2-phenyl-1H-indole
InChIKeyKLLLJCACIRKBDT-UHFFFAOYSA-N
INCHI1S/C14H11N/c1-2-6-11(7-3-1)14-10-12-8-4-5-9-13(12)15-14/h1-10,15H
Isomere SMILES C1=CC=C(C=C1)C2=CC3=CC=CC=C3N2
WGK Deutschland 3
RTECS NM1272500
Molekulargewicht 193.24
Beilstein 20467
Reaxy-Rn 132356
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=132356&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
KlasseIndoles and derivatives
SubclassIndoles
Intermediate Tree Nodes Not available
Direct Parent2-phenylindoles
Alternative Parents Phenylpyrroles  Benzene and substituted derivatives  Heteroaromatic compounds  Azacyclic compounds  Organopnictogen compounds  Organonitrogen compounds  Hydrocarbon derivatives  
Molecular FrameworkAromatic heteropolycyclic compounds
Substituents 2-phenylindole - 2-phenylpyrrole - Benzenoid - Substituted pyrrole - Monocyclic benzene moiety - Heteroaromatic compound - Pyrrole - Azacycle - Organic nitrogen compound - Organopnictogen compound - Hydrocarbon derivative - Organonitrogen compound - Aromatic heteropolycyclic compound
BeschreibungThis compound belongs to the class of organic compounds known as 2-phenylindoles. These are indoles substituted at the 2-position with a phenyl group.
External Descriptors Not available
3D-Struktur
Interaktives chemisches Strukturmodell





Zugehörige Ziele (menschlich)
CYP19A1 Tclin Cytochrome P450 19A1 (6099 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
PTH1R Tclin Parathyroid hormone receptor (47172 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
AKR1B1 Tclin Aldose reductase (1404 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HT-29 (80576 Activities)
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MCF7 (126967 Activities)
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U-251 (51189 Activities)
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U-87 MG (3946 Activities)
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HepG2 (196354 Activities)
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POLI Tchem DNA polymerase iota (116820 Activities)
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Liver (3974 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ERG Tbio Transcriptional regulator ERG (5589 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
NPC1 Tchem Niemann-Pick C1 protein (18985 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
RAB9A Tbio Ras-related protein Rab-9A (22488 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
microRNA 21 (64692 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ATAD5 Tbio ATPase family AAA domain-containing protein 5 (122566 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CDK1 Tchem Cyclin-dependent kinase 1/cyclin B (899 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
TARDBP Tchem TAR DNA-binding protein 43 (40113 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Zugehörige Ziele (nicht menschlich)
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)
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Acinetobacter baumannii (41033 Activities)
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Escherichia coli (133304 Activities)
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Bacillus cereus (7522 Activities)
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Plasmodium falciparum (966862 Activities)
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Cryptococcus neoformans (21258 Activities)
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Candida albicans (78123 Activities)
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Luciferin 4-monooxygenase (66902 Activities)
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Nqo1 NAD(P)H dehydrogenase [quinone] 1 (1058 Activities)
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norA Quinolone resistance protein norA (2171 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Txnrd1 Thioredoxin reductase 1, cytoplasmic (45279 Activities)
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Fusarium culmorum (260 Activities)
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Macrophomina phaseolina (474 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Rhizoctonia solani (2251 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Globisporangium debaryanum (107 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Rorc Nuclear receptor ROR-gamma (89407 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
FTL Ferritin light chain (43324 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Wirkungsmechanismen
Zertifikate (CoA, COO, BSE/TSE und Analyse-Diagramm)
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.

14 results found

Lot NumberCertificate TypeDatumArtikel
I2203415Certificate of AnalysisJun 11, 2026 P111467
I2203416Certificate of AnalysisJun 11, 2026 P111467
I2203417Certificate of AnalysisJun 11, 2026 P111467
I2203418Certificate of AnalysisJun 11, 2026 P111467
I2205122Certificate of AnalysisJun 11, 2026 P111467
G2215258Certificate of AnalysisApr 07, 2026 P111467
G1805112Certificate of AnalysisFeb 05, 2026 P111467
H2125361Certificate of AnalysisJun 09, 2025 P111467
H2125365Certificate of AnalysisJun 09, 2025 P111467
H2125366Certificate of AnalysisJun 09, 2025 P111467
H2125373Certificate of AnalysisJun 09, 2025 P111467
L2503364Certificate of AnalysisJul 04, 2024 P111467
D2324733Certificate of AnalysisAug 28, 2021 P111467
H2125374Certificate of AnalysisAug 28, 2021 P111467

Show more ⌵

Chemische und physikalische Eigenschaften
Siedepunkt (°C)250°C
Schmelzpunkt (°C)188-190°C
Molekulargewicht193.240 g/mol
XLogP33.800
Hydrogen Bond Donor Count1
Hydrogen Bond Acceptor Count0
Rotatable Bond Count1
Exact Mass193.089 Da
Monoisotopic Mass193.089 Da
Topological Polar Surface Area15.800 Ų
Heavy Atom Count15
Formal Charge0
Complexity207.000
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
Citations of This Product
Referenzen
1. Kang Feng, Chunhua Ni, Liangmin Yu, Wenjun Zhou, Xia Li.  (2019)  Synthesis and antifouling evaluation of indole derivatives.  ECOTOXICOLOGY AND ENVIRONMENTAL SAFETY,      [PMID:31325810] [10.1016/j.ecoenv.2019.109423]
Lösungsrechner
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Häufig gestellte Fragen

What is the purity of this product?
This product is supplied at ≥99% purity (chemical assay). Lot-specific values are stated on the Certificate of Analysis.
How should this product be stored?
Store at room temperature.
How is this product shipped?
This product ships under standard ambient conditions. No temperature-controlled packaging is required.
What are the CAS number, molecular formula and molecular weight?
The CAS Number is 948-65-2, the molecular formula is C14H11N, and the molecular weight is 193.24 g/mol. InChIKey KLLLJCACIRKBDT-UHFFFAOYSA-N.
What documentation is provided?
Available product documentation, including Certificates of Analysis (COA), Safety Data Sheets (SDS), and specification sheets, is shown in the product document area. Document availability and access follow the current site policy.

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