(E)-3-Methoxy-2-butenoic acid methyl ester - ≥95% , CAS No.4525-28-4

CAS: 4525-28-4 Cat. No.: E170426 Molecular Weight: 130.14 EC Number: 839-819-0

GRADE & PURITY ≥95%

Synonyms

methyl (2E)-3-methoxybut-2-enoate | (E)-3-Methoxy-2-butenoic acid methyl ester | AKOS006282711 | J-501965 | methyl (E)-3-methoxy-crotonate | EN300-1692916 | (E)-3-Methoxy-2-butenoic acid methyl ester, AldrichCPR | methyl (E)-3-methoxybut-2-enoate | (E)-3-

Storage

Store at 2-8°C

Shipped In

Wet ice

Specifications

Synonyms

methyl (2E)-3-methoxybut-2-enoate | (E)-3-Methoxy-2-butenoic acid methyl ester | AKOS006282711 | J-501965 | methyl (E)-3-methoxy-crotonate | EN300-1692916 | (E)-3-Methoxy-2-butenoic acid methyl ester, AldrichCPR | methyl (E)-3-methoxybut-2-enoate | (E)-3-

Specifications & Purity

≥95%

Legal Information

Product of Synthonix

Storage

Store at 2-8°C

Shipped In

Wet ice

This product requires cold chain shipping. Ground and other economy services are not available.

Purity

≥95%

Names and Identifiers

• Pubchem Sid: 504763690
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/504763690
• Canonical Smiles: CC(=CC(=O)OC)OC
• IUPAC Name: methyl (E)-3-methoxybut-2-enoate
• InChIKey: RJSHZZLJYZOHRU-SNAWJCMRSA-N
• INCHI: 1S/C6H10O3/c1-5(8-2)4-6(7)9-3/h4H,1-3H3/b5-4+
• Isomeric SMILES: C/C(=C\C(=O)OC)/OC
• WGK Germany: 3
• Molecular Weight: 130.14
• Reaxy-Rn: 1748814
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1748814&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Lipids and lipid-like molecules
    • Class Fatty Acyls
      • Subclass Fatty acid esters

• Kingdom: Organic compounds
• Superclass: Lipids and lipid-like molecules
• Class: Fatty Acyls
• Subclass: Fatty acid esters
• Intermediate Tree Nodes: Not available
• Direct Parent: Fatty acid esters
• Alternative Parents: Vinylogous esters Methyl esters Enoate esters Monocarboxylic acids and derivatives Organic oxides Hydrocarbon derivatives Carbonyl compounds
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Fatty acid ester - Vinylogous ester - Alpha,beta-unsaturated carboxylic ester - Enoate ester - Methyl ester - Carboxylic acid ester - Monocarboxylic acid or derivatives - Carboxylic acid derivative - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Carbonyl group - Aliphatic acyclic compound
• Description: This compound belongs to the class of organic compounds known as fatty acid esters. These are carboxylic ester derivatives of a fatty acid.
• 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

Chemical and Physical Properties

• Sensitivity: Moisture sensitive
• Molecular Weight: 130.139 g/mol
• XLogP3: 0.700
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 3
• Exact Mass: 130.063 Da
• Monoisotopic Mass: 130.063 Da
• Topological Polar Surface Area: 35.500 Ų
• Heavy Atom Count: 9
• Formal Charge: 0
• Complexity: 126.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 0
• Undefined Atom Stereocenter Count: 0
• Defined Bond Stereocenter Count: 1
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 1
• Covalently-Bonded Unit Count: 1