enow.com Web Search

Search results

  1. Results from the WOW.Com Content Network
  2. Amine - Wikipedia

    en.wikipedia.org/wiki/Amine

    Amine. In chemistry, amines (/ ə ˈ m iː n, ˈ æ m iː n /, [1] [2] UK also / ˈ eɪ m iː n / [3]) are compounds and functional groups that contain a basic nitrogen atom with a lone pair.Formally, amines are derivatives of ammonia (NH 3 (in which the bond angle between the nitrogen and hydrogen is 107°), wherein one or more hydrogen atoms have been replaced by a substituent such as an ...

  3. IUPAC nomenclature of organic chemistry - Wikipedia

    en.wikipedia.org/wiki/IUPAC_nomenclature_of...

    For secondary amines (of the form R−NH−R), the longest carbon chain attached to the nitrogen atom becomes the primary name of the amine; the other chain is prefixed as an alkyl group with location prefix given as an italic N: CH 3 NHCH 2 CH 3 is N-methylethanamine.

  4. Category:Tertiary amines - Wikipedia

    en.wikipedia.org/wiki/Category:Tertiary_amines

    Download as PDF; Printable version; In other projects Wikimedia Commons; ... Pages in category "Tertiary amines" The following 96 pages are in this category, out of ...

  5. Amide - Wikipedia

    en.wikipedia.org/wiki/Amide

    IUPAC recommends ethanamide, but this and related formal names are rarely encountered. When the amide is derived from a primary or secondary amine, the substituents on nitrogen are indicated first in the name. Thus, the amide formed from dimethylamine and acetic acid is N,N-dimethylacetamide (CH 3 CONMe 2, where Me = CH 3).

  6. Aminoaldehydes and aminoketones - Wikipedia

    en.wikipedia.org/wiki/Aminoaldehydes_and_aminoke...

    Because primary and secondary amines react with aldehydes and ketones, the most common variety of these aminocarbonyl compounds feature tertiary amines. Such compounds are produced by amination of α-haloketones and α-haloaldehydes. [1] Examples include cathinones, methadone, molindone, pimeclone, ferruginine, and tropinone.

  7. tert-Butylamine - Wikipedia

    en.wikipedia.org/wiki/Tert-Butylamine

    tert-Butylamine (also erbumine and other names) is an organic chemical compound with the formula (CH 3) 3 CNH 2.It is a colorless liquid with a typical amine-like odor. tert-Butylamine is one of the four isomeric amines of butane, the others being n-butylamine, sec-butylamine and isobutylamine.

  8. Mannich reaction - Wikipedia

    en.wikipedia.org/wiki/Mannich_reaction

    In the Mannich reaction, primary or secondary amines or ammonia react with formaldehyde to form a Schiff base. Tertiary amines lack an N–H proton and so do not react. The Schiff base can react with α-CH-acidic compounds (nucleophiles) that include carbonyl compounds, nitriles, acetylenes, aliphatic nitro compounds, α-alkyl-pyridines or imines.

  9. Category:Amines - Wikipedia

    en.wikipedia.org/wiki/Category:Amines

    Download as PDF; Printable version; ... Secondary amines (1 C, 115 P) ... Pages in category "Amines" The following 200 pages are in this category, out of ...