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· · COA & SDS Disponible para cada producto · Same-day shipping on in-stock items 7-Methylindole-3-carboxaldehyde - ≥98% , CAS No.4771-50-0
Synonyms
3-Carboxaldehyde, 7-methylindole- | AKOS005206800 | A15587 | EN300-1275516 | 7-Methylindole-3-aldehyde | 3-Formyl-7-methylindole | 7-Methylindole-3-carboxyaldehyde | DS-0060 | DTXSID20293694 | FT-0621463 | methyl5-(difluoromethoxy)-2-methylbenzoate | NSC9
Storage
Store at -20°C,Argon charged
Shipped In
Ice chest + Ice pads
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Why this grade ≥98% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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Storage & shipping Store at -20°C,Argon charged Ships Ice chest + Ice pads 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: 1.Tryptophan dioxygenase inhibitors pyridyl-ethenyl-indoles as potential anticancer immunomodulators. 2.Antibacterial and antituberculosis agents. 3.Antiandrogens effective against androgen receptor mutants. 4.Anti-bovine viral diarrhea virus (BVDV) agents. 5. Receptor subtype 5 antagonists. 6.Glucocorticoid receptor ligands. 7.Necroptosis inhibitors. 8. Orally efficacious small-molecule sctivator of the insulin receptor.
Specifications Sinónimos
3-Carboxaldehyde, 7-methylindole- | AKOS005206800 | A15587 | EN300-1275516 | 7-Methylindole-3-aldehyde | 3-Formyl-7-methylindole | 7-Methylindole-3-carboxyaldehyde | DS-0060 | DTXSID20293694 | FT-0621463 | methyl5-(difluoromethoxy)-2-methylbenzoate | NSC9
Especificaciones y pureza
≥98%
Condiciones de almacenamiento de almacenamiento
Store at -20°C, Argon charged
Enviado en
Ice chest + Ice pads
Este producto requiere envío en cadena de frío. Los servicios terrestres y otros servicios económicos no están disponibles.
Nombres e identificadores Sonrisas canónicas CC1=C2C(=CC=C1)C(=CN2)C=O IUPAC Name 7-methyl-1H-indole-3-carbaldehyde InChIKey KTUFZHVVJBHGKZ-UHFFFAOYSA-N INCHI 1S/C10H9NO/c1-7-3-2-4-9-8(6-12)5-11-10(7)9/h2-6,11H,1H3 Isómeros SMILES CC1=C2C(=CC=C1)C(=CN2)C=O WGK Alemania 3 Peso molecular 159.18 Reaxy-Rn 122340 Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=122340&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 Indoles Intermediate Tree Nodes Not available Direct Parent Indoles Alternative Parents Aryl-aldehydes Substituted pyrroles Benzenoids Vinylogous amides Heteroaromatic compounds Azacyclic compounds Organopnictogen compounds Organonitrogen compounds Organic oxides Hydrocarbon derivatives Molecular Framework Aromatic heteropolycyclic compounds Substituents Indole - Aryl-aldehyde - Substituted pyrrole - Benzenoid - Pyrrole - Heteroaromatic compound - Vinylogous amide - Azacycle - Aldehyde - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Organic oxygen compound - Organooxygen compound - Organonitrogen compound - Organic nitrogen compound - Aromatic heteropolycyclic compound Descripción This 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 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) Mecanismos de acción Certificados (CoA, COO, BSE/TSE y tabla de análisis) Propiedades químicas y físicas Sensibilidad Air Sensitive Punto de fusión (°C) 209-211°C Peso molecular 159.180 g/mol XLogP3 1.900 Hydrogen Bond Donor Count 1 Hydrogen Bond Acceptor Count 1 Rotatable Bond Count 1 Exact Mass 159.068 Da Monoisotopic Mass 159.068 Da Topological Polar Surface Area 32.900 Ų Heavy Atom Count 12 Formal Charge 0 Complexity 181.000 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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