2-(Methylthio)acetamide - ≥98%(GC) , CAS No.22551-24-2

CAS: 22551-24-2 Cat. No.: M158330 Summenformel: C₃H₇NOS Molekulargewicht: 105.16 EG-Nummer: 808-167-9

GRADE & PURITY ≥98%(GC)

Synonyms

C3H7NOS | AKOS008937723 | Acetamide, 2-(methylthio)- | ethyl2-(3,5-dimethoxyphenyl)acetate | J-506495 | EN300-1259143 | FT-0660513 | .alpha.-(Methylthio)acetamide | SY040648 | SCHEMBL158019 | Z33545668 | 2-(Methylsulfanyl)acetamide # | DTXSID50338249 | MF

Storage

Argon charged,Room temperature

Shipped In

Normal

Specifications

Synonyme

C3H7NOS | AKOS008937723 | Acetamide, 2-(methylthio)- | ethyl2-(3,5-dimethoxyphenyl)acetate | J-506495 | EN300-1259143 | FT-0660513 | .alpha.-(Methylthio)acetamide | SY040648 | SCHEMBL158019 | Z33545668 | 2-(Methylsulfanyl)acetamide # | DTXSID50338249 | MF

Spezifikationen & Reinheit

≥98%(GC)

Storage

Argon charged,Room temperature

Verschickt in

Normal

Reinheit

≥98%(GC)

Namen und Kennungen

• Pubchem Sid: 488190241
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/488190241
• Kanonisches Lächeln: CSCC(=O)N
• IUPAC Name: 2-methylsulfanylacetamide
• InChIKey: OBENGAMZEGRSIC-UHFFFAOYSA-N
• INCHI: 1S/C3H7NOS/c1-6-2-3(4)5/h2H2,1H3,(H2,4,5)
• Isomere SMILES: CSCC(=O)N
• Molekulargewicht: 105.16
• Reaxy-Rn: 1740197
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1740197&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic acids and derivatives
    • Klasse Carboxylic acids and derivatives
      • Subclass Carboxylic acid derivatives
        • Ebene5 Carboxylic acid amides
          • Ebene6 Primary carboxylic acid amides

• Kingdom: Organic compounds
• Superclass: Organic acids and derivatives
• Klasse: Carboxylic acids and derivatives
• Subclass: Carboxylic acid derivatives
• Intermediate Tree Nodes: Carboxylic acid amides
• Direct Parent: Primary carboxylic acid amides
• Alternative Parents: Sulfenyl compounds Dialkylthioethers Organopnictogen compounds Organonitrogen compounds Organic oxides Hydrocarbon derivatives Carbonyl compounds
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Primary carboxylic acid amide - Dialkylthioether - Sulfenyl compound - Thioether - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Organosulfur compound - Organooxygen compound - Organonitrogen compound - Carbonyl group - Aliphatic acyclic compound
• Beschreibung: This compound belongs to the class of organic compounds known as primary carboxylic acid amides. These are compounds comprising primary carboxylic acid amide functional group, with the general structure RC(=O)NH2.
• 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

Chemische und physikalische Eigenschaften

• Löslichkeit: Soluble in Methanol
• Empfindlichkeit: Moisture sensitive.
• Schmelzpunkt (°C): 102.0to106.0℃
• Molekulargewicht: 105.160 g/mol
• XLogP3: -0.200
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 2
• Exact Mass: 105.025 Da
• Monoisotopic Mass: 105.025 Da
• Topological Polar Surface Area: 68.400 Ų
• Heavy Atom Count: 6
• Formal Charge: 0
• Complexity: 54.800
• 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