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  2. Pentyl group - Wikipedia

    en.wikipedia.org/wiki/Pentyl_group

    Pentyl is a five-carbon alkyl group or substituent with chemical formula-C 5 H 11. It is the substituent form of the alkane pentane . In older literature, the common non-systematic name amyl was often used for the pentyl group.

  3. Alkyl group - Wikipedia

    en.wikipedia.org/wiki/Alkyl_group

    The prefixes taken from IUPAC nomenclature are used to name branched chained structures by their substituent groups, ... pentyl tert-pentyl tPe, t-Pe, t Pe

  4. Comparison of psychoactive alcohols in alcoholic drinks

    en.wikipedia.org/wiki/Comparison_of_psychoactive...

    IUPAC name Common name Classification CAS Ethanol: ... 0.07% in beer: 70 mg/100 mL (see tert-Pentyl alcohol in ref) Found in cassava fermented drinks: 1000 mg/kg

  5. tert-Amyl alcohol - Wikipedia

    en.wikipedia.org/wiki/Tert-Amyl_alcohol

    tert-Amyl alcohol (TAA) or 2-methylbutan-2-ol (2M2B), is a branched pentanol. Historically, TAA has been used as an anesthetic [3] and more recently as a recreational drug. [4] TAA is mostly a positive allosteric modulator for GABA A receptors in the same way as ethanol. [5] The psychotropic effects of TAA and ethanol are similar, though distinct.

  6. Amyl alcohol - Wikipedia

    en.wikipedia.org/wiki/Amyl_alcohol

    Amyl alcohol isomers; Common name Structure Type IUPAC name Boiling point (°C) [3] 1-pentanol or normal amyl alcohol primary Pentan-1-ol: 138.5 2-methyl-1-butanol or active amyl alcohol primary 2-Methylbutan-1-ol: 128.7 3-methyl-1-butanol or isoamyl alcohol or isopentyl alcohol primary 3-Methylbutan-1-ol: 131.2 2,2-dimethyl-1-propanol or ...

  7. Butyl group - Wikipedia

    en.wikipedia.org/wiki/Butyl_group

    The effect of the tert-butyl group on the progress of a chemical reaction is called the Thorpe–Ingold effect illustrated in the Diels-Alder reaction below. Compared to a hydrogen substituent, the tert-butyl substituent accelerates the reaction rate by a factor of 240. [2] tert-Butyl effect. The tert-butyl effect is an example of steric hindrance.

  8. Neopentyl alcohol - Wikipedia

    en.wikipedia.org/wiki/Neopentyl_alcohol

    Preferred IUPAC name. 2,2-Dimethylpropan-1-ol. Other names tert-Butyl carbinol tert-Butylmethanol ... The compound is one of the eight isomers of pentyl alcohol.

  9. IUPAC nomenclature of organic chemistry - Wikipedia

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

    ChemAxon Name <> Structure – ChemAxon IUPAC (& traditional) name to structure and structure to IUPAC name software. As used at chemicalize.org; chemicalize.org A free web site/service that extracts IUPAC names from web pages and annotates a 'chemicalized' version with structure images. Structures from annotated pages can also be searched.