5-Methoxy-1H-indole-3-carboxylic acid methyl ester - ≥97% , CAS No.172595-68-5

CAS: 172595-68-5 Cat. No.: M340541 Número EC: 989-579-7

GRADE & PURITY ≥97%

Synonyms

SCHEMBL5068806 | Methyl 5-methoxyindole-3-carboxylate | AKOS015851469 | AB1523 | 5-METHOXY-1H-INDOLE-3-CARBOXYLIC ACID METHYL ESTER | 5-Methoxyl-1H-3-Indole-carboxylicacid,, Methyl ester | methyl 5-methoxy-1H-indole-3-carboxylate | ODBFYEWPUQVAKY-UHFFFAOY

Storage

Room temperature

Shipped In

Normal

Specifications

Sinónimos

SCHEMBL5068806 | Methyl 5-methoxyindole-3-carboxylate | AKOS015851469 | AB1523 | 5-METHOXY-1H-INDOLE-3-CARBOXYLIC ACID METHYL ESTER | 5-Methoxyl-1H-3-Indole-carboxylicacid, , Methyl ester | methyl 5-methoxy-1H-indole-3-carboxylate | ODBFYEWPUQVAKY-UHFFFAOY

Especificaciones y pureza

≥97%

Condiciones de almacenamiento de almacenamiento

Room temperature

Enviado en

Normal

Pureza

≥97%

Nombres e identificadores

• Sonrisas canónicas: COC1=CC2=C(C=C1)NC=C2C(=O)OC
• IUPAC Name: methyl 5-methoxy-1H-indole-3-carboxylate
• InChIKey: ODBFYEWPUQVAKY-UHFFFAOYSA-N
• INCHI: 1S/C11H11NO3/c1-14-7-3-4-10-8(5-7)9(6-12-10)11(13)15-2/h3-6,12H,1-2H3
• Isómeros SMILES: COC1=CC2=C(C=C1)NC=C2C(=O)OC
• Reaxy-Rn: 13833028
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=13833028&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organoheterocyclic compounds
    • Clase Indoles and derivatives
      • Subclass Indolecarboxylic acids and derivatives

• 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 and derivatives Anisoles Alkyl aryl ethers Substituted pyrroles Vinylogous amides Methyl esters Heteroaromatic compounds Azacyclic compounds Organonitrogen compounds Organic oxides Hydrocarbon derivatives
• Molecular Framework: Aromatic heteropolycyclic compounds
• Substituents: Indolecarboxylic acid derivative - Indole - Anisole - Phenol ether - Pyrrole-3-carboxylic acid or derivatives - Alkyl aryl ether - Substituted pyrrole - Benzenoid - Heteroaromatic compound - Pyrrole - Vinylogous amide - Methyl ester - Carboxylic acid ester - Ether - Azacycle - Carboxylic acid derivative - Organic nitrogen compound - Organooxygen compound - Organonitrogen compound - Hydrocarbon derivative - Organic oxide - Organic oxygen 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: 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.

DOI: 10.1186/s13321-016-0174-y

Mecanismos de acción

Propiedades químicas y físicas

• Peso molecular: 205.210 g/mol
• XLogP3: 2.500
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 3
• Exact Mass: 205.074 Da
• Monoisotopic Mass: 205.074 Da
• Topological Polar Surface Area: 51.300 Ų
• Heavy Atom Count: 15
• Formal Charge: 0
• Complexity: 244.000
• 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