N-(Methoxymethyl)methacrylamide (stabilized with MEHQ) - ≥85%(GC) , CAS No.3644-12-0

CAS: 3644-12-0 Cat. No.: N159441 Peso molecular: 129.16 Número EC: 222-872-3

GRADE & PURITY ≥85%(GC)

Synonyms

YOZHLACIXDCHPV-UHFFFAOYSA-N | N-(Methoxymethyl)methacrylamide | AMY11203 | n-methoxymethyl methacrylamide | N-(Methoxymethyl)methacrylamide, >/=85%,stabilized with MEHQ | 2-Propenamide, N-(methoxymethyl)-2-methyl- | methoxymethylmethacrylamide | M2478 | W

Storage

Room temperature

Shipped In

Normal

Specifications

Sinónimos

YOZHLACIXDCHPV-UHFFFAOYSA-N | N-(Methoxymethyl)methacrylamide | AMY11203 | n-methoxymethyl methacrylamide | N-(Methoxymethyl)methacrylamide, >/=85%, stabilized with MEHQ | 2-Propenamide, N-(methoxymethyl)-2-methyl- | methoxymethylmethacrylamide | M2478 | W

Especificaciones y pureza

≥85%(GC)

Condiciones de almacenamiento de almacenamiento

Room temperature

Enviado en

Normal

Pureza

≥85%(GC)

Nombres e identificadores

• Sonrisas canónicas: CC(=C)C(=O)NCOC
• IUPAC Name: N-(methoxymethyl)-2-methylprop-2-enamide
• InChIKey: YOZHLACIXDCHPV-UHFFFAOYSA-N
• INCHI: 1S/C6H11NO2/c1-5(2)6(8)7-4-9-3/h1,4H2,2-3H3,(H,7,8)
• Isómeros SMILES: CC(=C)C(=O)NCOC
• Peso molecular: 129.16
• Reaxy-Rn: 1811802
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1811802&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic acids and derivatives
    • Clase Carboxylic acids and derivatives
      • Subclass Carboxylic acid derivatives
        • Level5 Carboxylic acid amides
          • Level6 Secondary carboxylic acid amides

• Kingdom: Organic compounds
• Superclass: Organic acids and derivatives
• Clase: Carboxylic acids and derivatives
• Subclass: Carboxylic acid derivatives
• Intermediate Tree Nodes: Carboxylic acid amides
• Direct Parent: Secondary carboxylic acid amides
• Alternative Parents: Organopnictogen compounds Organonitrogen compounds Organic oxides Hydrocarbon derivatives Carbonyl compounds
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Secondary carboxylic acid amide - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Organonitrogen compound - Carbonyl group - Aliphatic acyclic compound
• Descripción: This compound belongs to the class of organic compounds known as secondary carboxylic acid amides. These are compounds containing a secondary carboxylic acid amide functional group, with the general structure RC(=O)N(R')H (R,R'=alkyl, aryl).
• 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

• Índice de refracción: 1.47
• Punto de inflamación (°C): 105 °C
• Punto de ebullición (°C): 85°C/0.8mmHg(lit.)
• Peso molecular: 129.160 g/mol
• XLogP3: 0.500
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 3
• Exact Mass: 129.079 Da
• Monoisotopic Mass: 129.079 Da
• Topological Polar Surface Area: 38.300 Ų
• Heavy Atom Count: 9
• Formal Charge: 0
• Complexity: 120.000
• 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

Referencias

1. Xiao-Ye Lu, Qian-Yi Lv, Qi-Long Li, Hong Zhang, Chu-Tao Chen, Hao-Mei Tian.  (2024)  Impact of Acupuncture on Ischemia/Reperfusion Injury: Unraveling the Role of miR-34c-5p and Autophagy Activation.  BRAIN RESEARCH BULLETIN,      [PMID:39002935] [10.1016/j.brainresbull.2024.111031]