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CAS 1037184-07-8

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2,6-Dichloro-N-(2,6-dimethylphenyl)hexanamide

Description:
2,6-Dichloro-N-(2,6-dimethylphenyl)hexanamide is a synthetic organic compound characterized by its amide functional group, which is derived from hexanoic acid and features a dichloro substitution pattern on the aromatic ring. This compound typically exhibits a solid state at room temperature and is likely to be relatively stable under standard conditions. Its molecular structure includes a hexanamide backbone, which contributes to its potential solubility in organic solvents. The presence of the dichloro substituents and the dimethylphenyl group may influence its reactivity, making it of interest in various chemical applications, including pharmaceuticals and agrochemicals. The compound's specific properties, such as melting point, boiling point, and solubility, would depend on its molecular interactions and the presence of functional groups. Safety data sheets would provide essential information regarding its handling, toxicity, and environmental impact, which are crucial for any practical applications. Overall, 2,6-Dichloro-N-(2,6-dimethylphenyl)hexanamide represents a unique structure within the realm of organic chemistry.
Formula:C14H19Cl2NO
InChI:InChI=1S/C14H19Cl2NO/c1-10-6-5-7-11(2)13(10)17-14(18)12(16)8-3-4-9-15/h5-7,12H,3-4,8-9H2,1-2H3,(H,17,18)
InChI key:InChIKey=JHPMUNZBGKBWPW-UHFFFAOYSA-N
SMILES:N(C(C(CCCCCl)Cl)=O)C1=C(C)C=CC=C1C
Synonyms:
  • 2,6-Dichloro-N-(2,6-dimethylphenyl)hexanamide
  • Hexanamide, 2,6-dichloro-N-(2,6-dimethylphenyl)-
  • Bupivacaine EP Impurity D
  • Ropivacaine Dichloro Impurity
  • Bupivacaine Hydrochloride EP Impurity D
  • Bupivacaine - Impurity D (Freebase)
  • Bupivacaine Hydrochloride Impurity D
  • Levobupivacaine Impurity D
  • 2,6-dichlorocapronic acid xylidide
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