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  2. Acetamide - Wikipedia

    en.wikipedia.org/wiki/Acetamide

    Acetamide (systematic name: ethanamide) is an organic compound with the formula CH 3 CONH 2. It is an amide derived from ammonia and acetic acid . It finds some use as a plasticizer and as an industrial solvent. [ 5 ]

  3. Amide - Wikipedia

    en.wikipedia.org/wiki/Amide

    The structure of an amide can be described also as a resonance between two alternative structures: neutral (A) and zwitterionic (B). It is estimated that for acetamide , structure A makes a 62% contribution to the structure, while structure B makes a 28% contribution (these figures do not sum to 100% because there are additional less-important ...

  4. Dimethylacetamide - Wikipedia

    en.wikipedia.org/wiki/Dimethylacetamide

    The chemical reactions of dimethylacetamide are typical of N,N-disubstituted amides. Hydrolysis of the acyl-N bond occurs in the presence of acids: . CH 3 CON(CH 3) 2 + H 2 O + HCl → CH 3 COOH + (CH 3) 2 NH 2 + Cl −

  5. Iodoacetamide - Wikipedia

    en.wikipedia.org/wiki/Iodoacetamide

    Iodoacetamide (IAA) is an organic compound with the chemical formula I C H 2 CO NH 2.It is an alkylating agent used for peptide mapping purposes. Its actions are similar to those of iodoacetate.

  6. Bis(trimethylsilyl)acetamide - Wikipedia

    en.wikipedia.org/wiki/Bis(trimethylsilyl)acetamide

    Bis(trimethylsilyl)acetamide (BSA) is an organosilicon compound with the formula MeC(OSiMe 3)NSiMe 3 (Me = CH 3). It is a colorless liquid that is soluble in diverse organic solvents, but reacts rapidly with moisture and solvents containing OH and NH groups .

  7. Acetaldoxime - Wikipedia

    en.wikipedia.org/wiki/Acetaldoxime

    Acetaldoxime will often appear as a colorless liquid, or a white solid. Its solid can form two different needle-like crystal structures. The α-form melts at approximately 44 °C - 47 °C, while the β-form melts at 12 °C.

  8. Acyl group - Wikipedia

    en.wikipedia.org/wiki/Acyl_group

    Both are major contributors to the overall structure, so much so that the amide bond between the carbonyl carbon and the amide nitrogen has significant double bond character. The energy barrier for rotation about an amide bond is 75–85 kJ/mol (18–20 kcal/mol), much larger than values observed for normal single bonds.

  9. Sulfacetamide - Wikipedia

    en.wikipedia.org/wiki/Sulfacetamide

    Sulfacetamide is synthesized either by direct alkylation of acetamide with 4-aminobenzenesulfonyl chloride, or by reacting 4-aminobenzenesulfonamide with acetic anhydride and subsequent selective, reductive deacylation of the resultant acetamide using a system of zinc-sodium hydroxide. [27] [28]