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224,000+ productos de investigación · Triple ISO certified · COA & SDS Disponible para cada producto · Same-day shipping on in-stock items Indole-3-carboxylic Acid - 10mM in DMSO , CAS No.771-50-6
GRADE & PURITY 10mM in DMSO
Synonyms
EN300-13123 | FS-1053 | MFCD00005624 | 3-Indolecarboxylate | CCG-266287 | ICO | 3-Indolylcarboxylate | indole-3-carboxylate | 1H-Indole-3-carboxylic acid | EINECS 212-231-6 | Indole - 3 Carboxylic acid | 3-Indoleformate | F2147-0150 | Indole-3-carboxylic
Shipped In
Dry ice packs + Cold packs
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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.
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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.
Descripción general Reactant for preparation of: · Anticancer agents · Derivatives of amino acids and peptides · Serotonin 5-HT4 receptor antagonists · Primary acylureas · Inhibitors of Gli1-mediated transcription in the Hedgehog pathway · Serotonin 5-HT6 antagonists · Very Late Antigen-4 (VLA-4) sntagonists · EphB3 receptor tyrosine kinase inhibitors · Potential Therapeutic Agent for Alzheimer′s Disease · Vinyl ester pseudotripeptide proteasome inhibitors
Specifications Sinónimos
EN300-13123 | FS-1053 | MFCD00005624 | 3-Indolecarboxylate | CCG-266287 | ICO | 3-Indolylcarboxylate | indole-3-carboxylate | 1H-Indole-3-carboxylic acid | EINECS 212-231-6 | Indole - 3 Carboxylic acid | 3-Indoleformate | F2147-0150 | Indole-3-carboxylic
Especificaciones y pureza
10mM in DMSO
Condiciones de almacenamiento de almacenamiento
Store at -80°C
Enviado en
Dry ice packs + Cold packs
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Nombres e identificadores Sonrisas canónicas C1=CC=C2C(=C1)C(=CN2)C(=O)O IUPAC Name 1H-indole-3-carboxylic acid InChIKey KMAKOBLIOCQGJP-UHFFFAOYSA-N INCHI 1S/C9H7NO2/c11-9(12)7-5-10-8-4-2-1-3-6(7)8/h1-5,10H,(H,11,12) Isómeros SMILES C1=CC=C2C(=C1)C(=CN2)C(=O)O WGK Alemania 3 RTECS NK7882892 Peso molecular 161.16 Beilstein 129435 Reaxy-Rn 129435 Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=129435&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 Kingdom Organic compounds Superclass Organoheterocyclic compounds Clase Indoles and derivatives Subclass Indolecarboxylic acids and derivatives Intermediate Tree Nodes Not available Direct Parent Indolecarboxylic acids and derivatives Alternative Parents Indoles Pyrrole carboxylic acids Substituted pyrroles Benzenoids Vinylogous amides Heteroaromatic compounds Monocarboxylic acids and derivatives Carboxylic acids Azacyclic compounds Organopnictogen compounds Organooxygen compounds Organonitrogen compounds Organic oxides Hydrocarbon derivatives Molecular Framework Aromatic heteropolycyclic compounds Substituents Indolecarboxylic acid derivative - Indole - Pyrrole-3-carboxylic acid - Pyrrole-3-carboxylic acid or derivatives - Substituted pyrrole - Benzenoid - Pyrrole - Heteroaromatic compound - Vinylogous amide - Monocarboxylic acid or derivatives - Carboxylic acid derivative - Carboxylic acid - Azacycle - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Organooxygen compound - Organonitrogen compound - Organic oxygen compound - Organic nitrogen compound - Aromatic heteropolycyclic compound Descripción This 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 indol-3-yl carboxylic acid Data sources 1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.
Estructura 3D Objetivos asociados (humanos) Objetivos asociados (no humanos) Mecanismos de acción Certificados (CoA, COO, BSE/TSE y tabla de análisis) Propiedades químicas y físicas Punto de fusión (°C) 232-234°C Peso molecular 161.160 g/mol XLogP3 2.000 Hydrogen Bond Donor Count 2 Hydrogen Bond Acceptor Count 2 Rotatable Bond Count 1 Exact Mass 161.048 Da Monoisotopic Mass 161.048 Da Topological Polar Surface Area 53.100 Ų Heavy Atom Count 12 Formal Charge 0 Complexity 193.000 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
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