Indole-2-carboxylic Acid - 10mM in DMSO , CAS No.1477-50-5

CAS: 1477-50-5 Cat. No.: I421726 Peso molecular: 161.16 Beilstein Registry Number: 124132 Número EC: 216-030-4
Disponible para pedir
GRADE & PURITY 10mM in DMSO
Synonyms
Indole-2-carboxylicAcid-13C | MFCD00005611 | carboxyindole | FT-0627213 | BCP00082 | KBio2_004533 | Z56347139 | 1H-2-indolecarboxylic acid | 2-Indolecarboxylic acid | EN300-16592 | SMR000112260 | Spectrum_001485 | Carbon monoxide monosulfide | Indol-2-Car
Storage
Store at -80°C
Shipped In
Dry ice packs + Cold packs
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Size
Estado
Price
Qty
1ml
I421726-1ml
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58,90US$

69,90US$
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Why this grade

10mM in DMSO for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

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Storage & shipping

Store at -80°C Ships Dry ice packs + Cold packs 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 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Descripción general

Reactant for total synthesis of (±)-dibromophakellin and analogs,Reactant for synthesis of the pyrrolizidine alkaloid (±)-trachelanthamidine,Reactant for stereoselective preparation of renieramycin G analogs, Reactant for preparation of spirooxoindolepyrrolidines via reduction of indole-2-carboxylic acid followed by oxidation, condensation, reduction, amidation and Kharasch radical cyclization,Reactant for Pd-catalyzed cyclization,Reactant for preparation of N,N′-(pentane)diylbis[indolecarboxamide] and N,N′-[phenylenebis(methylene)]bis[indolecarboxamide] derivatives

Specifications

Sinónimos
Indole-2-carboxylicAcid-13C | MFCD00005611 | carboxyindole | FT-0627213 | BCP00082 | KBio2_004533 | Z56347139 | 1H-2-indolecarboxylic acid | 2-Indolecarboxylic acid | EN300-16592 | SMR000112260 | Spectrum_001485 | Carbon monoxide monosulfide | Indol-2-Car
Especificaciones y pureza
10mM in DMSO
Condiciones de almacenamiento de almacenamiento
Store at -80°C
Enviado en
Dry ice packs + Cold packs
Este producto requiere envío en cadena de frío. Los servicios terrestres y otros servicios económicos no están disponibles.
Nombres e identificadores
Sonrisas canónicasC1=CC=C2C(=C1)C=C(N2)C(=O)O
IUPAC Name1H-indole-2-carboxylic acid
InChIKeyHCUARRIEZVDMPT-UHFFFAOYSA-N
INCHI1S/C9H7NO2/c11-9(12)8-5-6-3-1-2-4-7(6)10-8/h1-5,10H,(H,11,12)
Isómeros SMILES C1=CC=C2C(=C1)C=C(N2)C(=O)O
WGK Alemania 3
Peso molecular 161.16
Beilstein 124132
Reaxy-Rn 124132
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=124132&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
ClaseIndoles and derivatives
SubclassIndolecarboxylic acids and derivatives
Intermediate Tree Nodes Not available
Direct ParentIndolecarboxylic acids and derivatives
Alternative Parents Indoles  Pyrrole 2-carboxylic acids  Substituted pyrroles  Benzenoids  Heteroaromatic compounds  Monocarboxylic acids and derivatives  Carboxylic acids  Azacyclic compounds  Organopnictogen compounds  Organooxygen compounds  Organonitrogen compounds  Organic oxides  Hydrocarbon derivatives  
Molecular FrameworkAromatic heteropolycyclic compounds
Substituents Indolecarboxylic acid derivative - Indole - Pyrrole-2-carboxylic acid - Pyrrole-2-carboxylic acid or derivatives - Substituted pyrrole - Benzenoid - Pyrrole - Heteroaromatic compound - Carboxylic acid derivative - Carboxylic acid - Monocarboxylic acid or derivatives - Azacycle - Organooxygen compound - Organonitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Organic nitrogen compound - Aromatic heteropolycyclic compound
DescripciónThis compound belongs to the class of organic compounds known as indolecarboxylic acids and derivatives. These are compounds containing a carboxylic acid group (or a derivative thereof) linked to an indole.
External Descriptors Not available
Estructura 3D
Modelo de Estructura Química Interactiva





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Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
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Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
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DDO Tchem D-aspartate oxidase (120 Activities)
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SLCO1B3 Tchem Solute carrier organic anion transporter family member 1B3 (2517 Activities)
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USP1 Tchem Ubiquitin carboxyl-terminal hydrolase 1 (22556 Activities)
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Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
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Mecanismos de acción
Certificados (CoA, COO, BSE/TSE y tabla de análisis)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:
Propiedades químicas y físicas
Sensibilidadair sensitive
Punto de fusión (°C)202-206°C
Peso molecular161.160 g/mol
XLogP32.300
Hydrogen Bond Donor Count2
Hydrogen Bond Acceptor Count2
Rotatable Bond Count1
Exact Mass161.048 Da
Monoisotopic Mass161.048 Da
Topological Polar Surface Area53.100 Ų
Heavy Atom Count12
Formal Charge0
Complexity193.000
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
Preguntas frecuentes y artículos
Calculadoras de soluciones
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