Pivalamide - ≥98% , CAS No.754-10-9

CAS: 754-10-9 Cat. No.: P160454 Summenformel: C₅H₁₁NO Molekulargewicht: 101.15 Beilstein Registry Number: 2320 EG-Nummer: 212-043-4 PubChem CID: 12957

QUALITÄT & REINHEIT ≥98%

Synonyms

neopentanamide | 2,2,2-Trimethylacetamide | P0819 | HMS1763O22 | XIPFMBOWZXULIA-UHFFFAOYSA- | A9605 | NSC17584 | NSC-17584 | pivalic acid amide | AC-907/25014088 | TAY | NSC 17584 | .ALPHA.,.ALPHA.-DIMETHYLPROPIONAMIDE | FES86MR7ZI | Propanamide, 2,2-dime

Storage

Room temperature

Shipped In

Normal

Spezifikationen

Synonyme

neopentanamide | 2,2,2-Trimethylacetamide | P0819 | HMS1763O22 | XIPFMBOWZXULIA-UHFFFAOYSA- | A9605 | NSC17584 | NSC-17584 | pivalic acid amide | AC-907/25014088 | TAY | NSC 17584 | .ALPHA.,.ALPHA.-DIMETHYLPROPIONAMIDE | FES86MR7ZI | Propanamide, 2,2-dime

Spezifikationen & Reinheit

≥98%

Storage

Room temperature

Verschickt in

Normal

Reinheit

≥98%

Namen und Kennungen

Pubchem Sid

488181754

Pubchem Sid Url

https://pubchem.ncbi.nlm.nih.gov/substance/488181754

Kanonisches Lächeln

CC(C)(C)C(=O)N

IUPAC Name

2,2-dimethylpropanamide

InChIKey

XIPFMBOWZXULIA-UHFFFAOYSA-N

INCHI

1S/C5H11NO/c1-5(2,3)4(6)7/h1-3H3,(H2,6,7)

Isomere SMILES

CC(C)(C)C(=O)N

WGK Deutschland

3

PubChem CID

12957

Molekulargewicht

101.15

Beilstein

2320

Reaxy-Rn

1742147

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: Organopnictogen compounds Organonitrogen compounds Organic oxides Hydrocarbon derivatives Carbonyl compounds
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Primary carboxylic acid amide - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - 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

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Mus musculus (284745 Activities)

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Wirkungsmechanismen

Chemische und physikalische Eigenschaften

• Siedepunkt (°C): 212 °C
• Schmelzpunkt (°C): 153 - 157°C
• Molekulargewicht: 101.150 g/mol
• XLogP3: 0.500
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 1
• Exact Mass: 101.084 Da
• Monoisotopic Mass: 101.084 Da
• Topological Polar Surface Area: 43.100 Ų
• Heavy Atom Count: 7
• Formal Charge: 0
• Complexity: 80.600
• 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