Methyl Indole-5-carboxylate - ≥98%(HPLC) , CAS No.1011-65-0

CAS: 1011-65-0 Cat. No.: M158570 Molecular Weight: 175.19 Beilstein Registry Number: 22(5)3,44 EC Number: 627-947-8
AVAILABLE TO ORDER
GRADE & PURITY ≥98%(HPLC)
Synonyms
Indole-5-carboxylic Acid Methyl Ester | 5-Indolecarboxylicacidmethylester | 5-methoxycarbonylindole | MFCD00153023 | PB29029 | AC-3031 | Indole-5-carboxylate | 1H-Indole-5-carboxylic acid methyl ester | 1H-Indole-5-carboxylic acid, methyl ester | BDBM9301
Storage
Room temperature
Shipped In
Normal
 ·  off list, applied to all prices below.
Size
Status
Price
Qty
200mg
M158570-200mg
3

$9.90

$14.90
Save $5.00 (33.56%)
1g
M158570-1g
6

$16.90

$25.90
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5g
M158570-5g
5

$26.90

$40.90
Save $14.00 (34.23%)
25g
M158570-25g
4

$71.90

$107.90
Save $36.00 (33.36%)
100g
M158570-100g
2

$284.90

$427.90
Save $143.00 (33.42%)
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Why this grade

≥98%(HPLC) 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.

Specifications

Synonyms
Indole-5-carboxylic Acid Methyl Ester | 5-Indolecarboxylicacidmethylester | 5-methoxycarbonylindole | MFCD00153023 | PB29029 | AC-3031 | Indole-5-carboxylate | 1H-Indole-5-carboxylic acid methyl ester | 1H-Indole-5-carboxylic acid, methyl ester | BDBM9301
Specifications & Purity
≥98%(HPLC)
Storage
Room temperature
Shipped In
Normal
Purity
≥98%(HPLC)
Names and Identifiers
Pubchem Sid488192920
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/488192920
Canonical SmilesCOC(=O)C1=CC2=C(C=C1)NC=C2
IUPAC Namemethyl 1H-indole-5-carboxylate
InChIKeyDRYBMFJLYYEOBZ-UHFFFAOYSA-N
INCHI1S/C10H9NO2/c1-13-10(12)8-2-3-9-7(6-8)4-5-11-9/h2-6,11H,1H3
Isomeric SMILES COC(=O)C1=CC2=C(C=C1)NC=C2
WGK Germany 3
Molecular Weight 175.19
Beilstein 22(5)3,44
Reaxy-Rn 474256
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=474256&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.

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🔬 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
SubclassIndolecarboxylic acids and derivatives
Intermediate Tree Nodes Not available
Direct ParentIndolecarboxylic acids
Alternative Parents Indoles  Benzenoids  Pyrroles  Methyl esters  Heteroaromatic compounds  Monocarboxylic acids and derivatives  Azacyclic compounds  Organopnictogen compounds  Organooxygen compounds  Organonitrogen compounds  Organic oxides  Hydrocarbon derivatives  
Molecular FrameworkAromatic heteropolycyclic compounds
Substituents Indolecarboxylic acid - Indole - Benzenoid - Pyrrole - Methyl ester - Heteroaromatic compound - Carboxylic acid ester - Azacycle - Carboxylic acid derivative - Monocarboxylic acid or derivatives - Organopnictogen compound - Organooxygen compound - Organonitrogen compound - Organic oxygen compound - Organic nitrogen compound - Hydrocarbon derivative - Organic oxide - Aromatic heteropolycyclic compound
DescriptionThis compound belongs to the class of organic compounds known as indolecarboxylic acids. These are compounds containing a carboxylic acid group linked to an indole.
External Descriptors Not available
3D Structure
Interactive Chemical Structure Model





Associated Targets(Human)
PTH1R Tclin Parathyroid hormone receptor (47172 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
FEN1 Tchem Flap endonuclease 1 (12055 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
POLI Tchem DNA polymerase iota (116820 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
TDP1 Tchem Tyrosyl-DNA phosphodiesterase 1 (345557 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
CDK5 Tchem Cyclin-dependent kinase 5/CDK5 activator 1 (3697 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
GSK3A Tclin Glycogen synthase kinase-3 (736 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Associated Targets(non-human)
Plasmodium falciparum (966862 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Luciferin 4-monooxygenase (66902 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.

13 results found

Lot NumberCertificate TypeDateItem
E2626146Certificate of AnalysisMay 29, 2026 M158570
E23061114Certificate of AnalysisFeb 05, 2026 M158570
E23061125Certificate of AnalysisFeb 05, 2026 M158570
E23061129Certificate of AnalysisFeb 05, 2026 M158570
E23061130Certificate of AnalysisFeb 05, 2026 M158570
E23061138Certificate of AnalysisFeb 05, 2026 M158570
E2306556Certificate of AnalysisFeb 05, 2026 M158570
E2306561Certificate of AnalysisFeb 05, 2026 M158570
E2306563Certificate of AnalysisFeb 05, 2026 M158570
G2418253Certificate of AnalysisJul 25, 2024 M158570
G2418628Certificate of AnalysisJul 25, 2024 M158570
G2418229Certificate of AnalysisApr 26, 2024 M158570
C2425069Certificate of AnalysisMar 30, 2024 M158570

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Chemical and Physical Properties
SolubilityInsoluble in water.
Melt Point(°C)125-129℃
Molecular Weight175.180 g/mol
XLogP32.600
Hydrogen Bond Donor Count1
Hydrogen Bond Acceptor Count2
Rotatable Bond Count2
Exact Mass175.063 Da
Monoisotopic Mass175.063 Da
Topological Polar Surface Area42.100 Ų
Heavy Atom Count13
Formal Charge0
Complexity205.000
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
References
1. Xiang Xu, Yi Shen, Yue Shu, Yong Guan, Dafu Wei.  (2022)  Synthesis and application of poly methyl indole-4-carboxylate with blue light blocking properties.  EUROPEAN POLYMER JOURNAL,      [PMID:] [10.1016/j.eurpolymj.2022.111198]
Solution Calculators
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