Glycidic Acid Methyl Ester - ≥98% , CAS No.4538-50-5

CAS: 4538-50-5 Cat. No.: G303748 Peso molecular: 102.09 Número EC: 610-247-1

GRADE & PURITY ≥98%

Synonyms

methyl oxirane-2-carboxylate|4538-50-5|Glycidic acid methyl ester|Methyl glycidate|Oxiranecarboxylic acid, methyl ester|methyl 2,3-epoxypropionate|Methyl-2,3-epoxypropanoate|MFCD17676228|Cucurbitaceae|bitter cucumber|Methyl (2S)-2,3-epoxypropanoate|MFCD00

Storage

Store at -20°C,Argon charged

Shipped In

Ice chest + Ice pads

Specifications

Sinónimos

methyl oxirane-2-carboxylate | 4538-50-5 | Glycidic acid methyl ester | Methyl glycidate | Oxiranecarboxylic acid, methyl ester | methyl 2, 3-epoxypropionate | Methyl-2, 3-epoxypropanoate | MFCD17676228 | Cucurbitaceae | bitter cucumber | Methyl (2S)-2, 3-epoxypropanoate | MFCD00

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.

Pureza

≥98%

Nombres e identificadores

• Pubchem Sid: 504757291
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/504757291
• Sonrisas canónicas: COC(=O)C1CO1
• IUPAC Name: methyl oxirane-2-carboxylate
• InChIKey: YKNYRRVISWJDSR-UHFFFAOYSA-N
• INCHI: 1S/C4H6O3/c1-6-4(5)3-2-7-3/h3H,2H2,1H3
• Isómeros SMILES: COC(=O)C1CO1
• Peso molecular: 102.09
• Reaxy-Rn: 1281012
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1281012&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organoheterocyclic compounds
    • Clase Epoxides
      • Subclass Oxirane carboxylic acids and derivatives

• Kingdom: Organic compounds
• Superclass: Organoheterocyclic compounds
• Clase: Epoxides
• Subclass: Oxirane carboxylic acids and derivatives
• Intermediate Tree Nodes: Not available
• Direct Parent: Oxirane carboxylic acids
• Alternative Parents: Methyl esters Oxacyclic compounds Monocarboxylic acids and derivatives Dialkyl ethers Organic oxides Hydrocarbon derivatives Carbonyl compounds
• Molecular Framework: Aliphatic heteromonocyclic compounds
• Substituents: Oxirane carboxylic acid - Methyl ester - Carboxylic acid ester - Oxacycle - Monocarboxylic acid or derivatives - Ether - Dialkyl ether - Carboxylic acid derivative - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Carbonyl group - Aliphatic heteromonocyclic compound
• Descripción: This compound belongs to the class of organic compounds known as oxirane carboxylic acids. These are compounds containing an oxirane ring bearing a carboxylic acid group.
• 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

Propiedades químicas y físicas

• Solubilidad: Chloroform (Slightly), Methanol (Slightly)
• Punto de fusión (°C): >300°C
• Peso molecular: 102.090 g/mol
• XLogP3: -0.200
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 2
• Exact Mass: 102.032 Da
• Monoisotopic Mass: 102.032 Da
• Topological Polar Surface Area: 38.800 Ų
• Heavy Atom Count: 7
• Formal Charge: 0
• Complexity: 88.900
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 0
• Undefined Atom Stereocenter Count: 1
• Defined Bond Stereocenter Count: 0
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 0
• Covalently-Bonded Unit Count: 1