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  2. 1-Aminopentane - Wikipedia

    en.wikipedia.org/wiki/1-aminopentane

    1-Aminopentane is an organic compound with the formula CH 3 (CH 2) ... Pentylamine exhibits reactions typical of other simple alkyl amines, i.e. protonation ...

  3. α-Propylphenethylamine - Wikipedia

    en.wikipedia.org/wiki/Α-Propylphenethylamine

    α-Propylphenethylamine (APPEA or α-Pr-PEA), also known as 1-phenyl-2-aminopentane, is a stimulant drug of the phenethylamine and amphetamine families. [1] [2] It is the analogue of the β-phenethylamine (PEA) derivatives amphetamine (α-methylphenethylamine; "AMPEA") and phenylisobutylamine (α-ethylphenethylamine; AEPEA) in which the α-alkyl chain has been further lengthened to be a propyl ...

  4. 1,3-Benzodioxolylpentanamine - Wikipedia

    en.wikipedia.org/wiki/1-(3,4-Methylenedioxy...

    1,3-Benzodioxolylpentanamine (BDP), also known as K or as 3,4-methylenedioxy-α-propylphenethylamine (MDPPEA), is a drug of the phenethylamine and amphetamine families. [ 1 ] [ 2 ] [ 3 ] It is the parent compound of 1,3-benzodioxolyl- N -methylpentanamine (MBDP; methyl-K) and 1,3-benzodioxolyl- N -ethylpentanamine (EBDP; ethyl-K), as well as of ...

  5. Aminopentane - Wikipedia

    en.wikipedia.org/wiki/Aminopentane

    Aminopentane may refer to: 1-Aminopentane; 2-Aminopentane; 3-Aminopentane This page was last edited on 4 August 2019, at 16:05 (UTC). Text is available under the ...

  6. 4,7-Dichloroquinoline - Wikipedia

    en.wikipedia.org/wiki/4,7-Dichloroquinoline

    The chlorine atom in the 4-position in the pyridine ring is much more reactive in nucleophilic aromatic substitution reactions [9] than the chlorine in the benzene ring. As a result, it can be replaced selectively to form derivatives at that position. A typical reaction with a specific primary amine gives chloroquine in high yield: [6] [7]

  7. Stevens rearrangement - Wikipedia

    en.wikipedia.org/wiki/Stevens_rearrangement

    The reaction mechanism of the Stevens rearrangement is one of the most controversial reaction mechanisms in organic chemistry. [4] Key in the reaction mechanism [5] [6] for the Stevens rearrangement (explained for the nitrogen reaction) is the formation of an ylide after deprotonation of the ammonium salt by a strong base.

  8. Sharon Stone Reveals Unexpected Family Link to Royalty - AOL

    www.aol.com/sharon-stone-reveals-unexpected...

    Sharon Stone "feels particularly good" after finding out that she has royal blood in her veins.. The actress recently appeared on the TV series Finding Your Roots, which looks at the ancestry of ...

  9. C5H13N - Wikipedia

    en.wikipedia.org/wiki/C5H13N

    1-Aminopentane; 3-Aminopentane; N,N-Diethylmethylamine; N-Methylisobutylamine; Neopentylamine This page was last edited on 14 December 2023, at 00 ...