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6-Methoxyindole - ≥98%(GC) , CAS No.3189-13-7

CAS: 3189-13-7 Cat. No.: M123429 Molecular Weight: 147.17 Beilstein Registry Number: 116483 EC Number: 221-689-6
COA
6-Methoxyindole - ≥98%(GC) CAS No(3189-13-7) by Aladdin Scientific
AVAILABLE TO ORDER
GRADE & PURITY ≥98%(GC)
Synonyms
NSC 92517 | 6-Methoxy indole | ethyl-o-toluate | MLS000689267 | STK893352 | 4-Bromo Phthalic anhydride | 6-Methoxy-1H-indole | chloroxoquinoline | 1H-Indol-6-yl methyl ether | HMS2718O18 | NCGC00245927-01 | FT-0621193 | 6-Methoxyindole | AQ-776/40228276 |
Storage
Protected from light,Argon charged,Room temperature
Shipped In
Normal
★
Size
Status
Price
Qty
250mg
M123429-250mg
3

$9.90

$14.90
Save $5.00 (33.56%)
1g
M123429-1g
3

$11.90

$17.90
Save $6.00 (33.52%)
5g
M123429-5g
3

$17.90

$26.90
Save $9.00 (33.46%)
10g
M123429-10g
8-12 wks(?) Production requires sourcing of materials. We appreciate your patience and understanding.

$22.90

$34.90
Save $12.00 (34.38%)
25g
M123429-25g
3

$55.90

$83.90
Save $28.00 (33.37%)
100g
M123429-100g
2

$222.90

$334.90
Save $112.00 (33.44%)
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SDS
Safety data
COA
Certificate
DS
Datasheet
SP
Spec sheet
Overview Specifications Names and Identifiers Documentation Advanced Data Taxonomic Classification 3D Structure Associated Targets(Human) Associated Targets(non-human) Mechanisms of Action Certificates（CoA,COO,BSE/TSE and Analysis Chart) Chemical and Physical Properties Solution Calculators Reviews
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Why this grade

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

🌡

Storage & shipping

Protected from light,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.

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Literature proof

Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Overview

Reactant for preparation of tryptophan dioxygenase inhibitors pyridyl-ethenyl-indoles as potential anticancer immunomodulators.and for synthesis of indolylindazoles and indolylpyrazolopyridines as interleukin-2 inducible T cell kinase inhibitors.and for preparation of diindolyloxyindoles as anticancer agents.

Specifications

Synonyms
NSC 92517 | 6-Methoxy indole | ethyl-o-toluate | MLS000689267 | STK893352 | 4-Bromo Phthalic anhydride | 6-Methoxy-1H-indole | chloroxoquinoline | 1H-Indol-6-yl methyl ether | HMS2718O18 | NCGC00245927-01 | FT-0621193 | 6-Methoxyindole | AQ-776/40228276 |
Specifications & Purity
≥98%(GC)
Biochemical and Physiological Mechanisms
6-Methoxyindole inhibits the chlorinating activity of myeloperoxidase and inhibits the generation of hypochlorous acid released by activated leukocytes.
Storage
Protected from light, Argon charged, Room temperature
Shipped In
Normal
Purity
≥98%(GC)
Names and Identifiers
Pubchem Sid504755089
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/504755089
Canonical SmilesCOC1=CC2=C(C=C1)C=CN2
IUPAC Name6-methoxy-1H-indole
InChIKeyQJRWYBIKLXNYLF-UHFFFAOYSA-N
INCHI1S/C9H9NO/c1-11-8-3-2-7-4-5-10-9(7)6-8/h2-6,10H,1H3
Isomeric SMILES COC1=CC2=C(C=C1)C=CN2
WGK Germany 3
Molecular Weight 147.17
Beilstein 116483
Reaxy-Rn 116483
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=116483&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.

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📊 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
SubclassIndoles
Intermediate Tree Nodes Not available
Direct ParentIndoles
Alternative Parents Anisoles  Alkyl aryl ethers  Pyrroles  Heteroaromatic compounds  Azacyclic compounds  Organopnictogen compounds  Organonitrogen compounds  Hydrocarbon derivatives  
Molecular FrameworkAromatic heteropolycyclic compounds
Substituents Indole - Anisole - Alkyl aryl ether - Benzenoid - Heteroaromatic compound - Pyrrole - Azacycle - Ether - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Hydrocarbon derivative - Organooxygen compound - Organonitrogen compound - Aromatic heteropolycyclic compound
DescriptionThis compound belongs to the class of organic compounds known as indoles. These are compounds containing an indole moiety, which consists of pyrrole ring fused to benzene to form 2,3-benzopyrrole.
External Descriptors Not available
3D Structure
Interactive Chemical Structure Model





Associated Targets(Human)
VDR Tclin Vitamin D receptor (26531 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ACHE Tclin Acetylcholinesterase (18204 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
POLB Tchem DNA polymerase beta (23632 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
PLK1 Tchem Serine/threonine-protein kinase PLK1 (28605 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HEK293 (82097 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
POLI Tchem DNA polymerase iota (116820 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
KDM4A Tchem Lysine-specific demethylase 4A (52245 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SMAD3 Tchem Mothers against decapentaplegic homolog 3 (68039 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
RGS4 Tchem Regulator of G-protein signaling 4 (13867 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Associated Targets(non-human)
Mapk1 MAP kinase ERK2 (650 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Plasmodium falciparum (966862 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.

7 results found

Lot NumberCertificate TypeDateItem
C2617186Certificate of AnalysisMar 25, 2026 M123429
C2209079Certificate of AnalysisDec 10, 2025 M123429
C2209082Certificate of AnalysisDec 10, 2025 M123429
C2209083Certificate of AnalysisDec 10, 2025 M123429
G2425497Certificate of AnalysisJun 24, 2024 M123429
H1504097Certificate of AnalysisApr 12, 2023 M123429
F2412037Certificate of AnalysisFeb 08, 2022 M123429
Chemical and Physical Properties
SensitivityLight Sensitive;Air sensitive
Boil Point(°C)105°C/0.2mm
Melt Point(°C)90-94°C
Molecular Weight147.170 g/mol
XLogP32.600
Hydrogen Bond Donor Count1
Hydrogen Bond Acceptor Count1
Rotatable Bond Count1
Exact Mass147.068 Da
Monoisotopic Mass147.068 Da
Topological Polar Surface Area25.000 Ų
Heavy Atom Count11
Formal Charge0
Complexity138.000
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
Solution Calculators
Reviews

Customer Reviews

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