N-Methyltrifluoroacetamide - ≥98%(GC) , CAS No.815-06-5

CAS: 815-06-5 Cat. No.: M123387 Peso molecular: 127.07 Beilstein Registry Number: 1703392 Número EC: 212-417-7

GRADE & PURITY ≥98%(GC)

Synonyms

methyltrifluoroacetamide | Acetamide, 2,2,2-trifluoro-N-methyl- | N-Methyl-2,2,2-trifluoroacetamide | N-Methyltrifluoroacetamide | 2,2,2-trifluoro-N-methyl-acetamide | n-methyl trifluoroacetamide | 2,2,2-Trifluoro-N-methylacetamide

Storage

Room temperature,Argon charged

Shipped In

Normal

Specifications

Sinónimos

methyltrifluoroacetamide | Acetamide, 2, 2, 2-trifluoro-N-methyl- | N-Methyl-2, 2, 2-trifluoroacetamide | N-Methyltrifluoroacetamide | 2, 2, 2-trifluoro-N-methyl-acetamide | n-methyl trifluoroacetamide | 2, 2, 2-Trifluoro-N-methylacetamide

Especificaciones y pureza

≥98%(GC)

Condiciones de almacenamiento de almacenamiento

Room temperature, Argon charged

Enviado en

Normal

Pureza

≥98%(GC)

Nombres e identificadores

• Pubchem Sid: 504754466
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/504754466
• Sonrisas canónicas: CNC(=O)C(F)(F)F
• IUPAC Name: 2,2,2-trifluoro-N-methylacetamide
• InChIKey: IQNHBUQSOSYAJU-UHFFFAOYSA-N
• INCHI: 1S/C3H4F3NO/c1-7-2(8)3(4,5)6/h1H3,(H,7,8)
• Isómeros SMILES: CNC(=O)C(F)(F)F
• WGK Alemania: 3
• Peso molecular: 127.07
• Beilstein: 1703392
• Reaxy-Rn: 1703392
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1703392&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 Organofluorides Organic oxides Hydrocarbon derivatives Carbonyl compounds Alkyl fluorides
• 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 - Organofluoride - Organohalogen compound - Carbonyl group - Alkyl halide - Alkyl fluoride - 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

• Sensibilidad: Hygroscopic
• Punto de inflamación (°F): 165.2 °F
• Punto de inflamación (°C): 73°C(163°F)
• Punto de ebullición (°C): 160°C
• Punto de fusión (°C): 49-52°C
• Peso molecular: 127.070 g/mol
• XLogP3: 0.700
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 0
• Exact Mass: 127.024 Da
• Monoisotopic Mass: 127.024 Da
• Topological Polar Surface Area: 29.100 Ų
• Heavy Atom Count: 8
• Formal Charge: 0
• Complexity: 97.200
• 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. Yuanxin Gao, Xinyi Wang, Dong Lv, Zhang Zhang, Jiangpeng Li, Xiaoyan Feng, Jingchao Chai, Yun Zheng, Yu Peng, Yanqing Wang, Yingying Wang, Lingyu Zhu, Zhihong Liu.  (2025)  Fluorination Engineering for Stable Interfacial Chemistry in Deep Eutectic Amide-Based Electrolytes Enables High-Performance LiNi0.8Co0.1Mn0.1O2/Li Batteries.  Energy & Environmental Materials,      [PMID:] [10.1002/eem2.70157]