CAS 5579-13-5
:N-(Aminocarbonyl)-2-ethyl-3-methylpentanamide
Description:
N-(Aminocarbonyl)-2-ethyl-3-methylpentanamide, with the CAS number 5579-13-5, is an organic compound characterized by its amide functional group, which is indicative of its potential as a building block in organic synthesis and pharmaceuticals. This compound features a branched alkyl chain, contributing to its hydrophobic characteristics, while the aminocarbonyl group enhances its reactivity and solubility in polar solvents. The presence of both ethyl and methyl groups in its structure suggests that it may exhibit unique steric and electronic properties, influencing its interactions in biological systems. As an amide, it may participate in hydrogen bonding, which can affect its boiling point and solubility. The compound's stability and reactivity can be influenced by the surrounding functional groups and the overall molecular structure. While specific applications may vary, compounds of this nature are often explored in medicinal chemistry for their potential therapeutic effects or as intermediates in the synthesis of more complex molecules.
Formula:C9H18N2O2
InChI:InChI=1S/C9H18N2O2/c1-4-6(3)7(5-2)8(12)11-9(10)13/h6-7H,4-5H2,1-3H3,(H3,10,11,12,13)
InChI key:InChIKey=HLSLSXBFTXUKCY-UHFFFAOYSA-N
SMILES:C(C(NC(N)=O)=O)(C(CC)C)CC
Synonyms:- N-carbamoyl-2-ethyl-3-methylpentanamide
- Capurida [INN-Spanish]
- Capuride [USAN:INN]
- (2-Ethyl-3-methylvaleryl)urea
- Pentanamide, N-(aminocarbonyl)-2-ethyl-3-methyl-
- (2-Ethyl-3-methylvaleryl)urea
- McN-X 94
- Capuridum [INN-Latin]
- NSC 27178
- Capuridum
- Urea, (2-ethyl-3-methylvaleryl)- (8CI)
- UNII-3FO9QT93IS
- 1-(2-Ethyl-3-methylpentanoyl)urea
- Capurida
- Pentanamide, N-(aminocarbonyl)-2-ethyl-3-methyl-
- Urea, (2-ethyl-3-methylvaleryl)-
- N-(Aminocarbonyl)-2-ethyl-3-methylpentanamide
- Capurid
- (Ethyl-sec-butylacetyl)urea
- Pacinox
- NSC 27690
- Capuride
- Urea, (2-ethyl-3-methyl-valeryl)-
- McN-X-94
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