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  2. 1-Chloropentane - Wikipedia

    en.wikipedia.org/wiki/1-Chloropentane

    Names Preferred IUPAC name. 1-Chloropentane. Other names n-Pentyl chloride; n-Amyl chloride. Identifiers CAS Number. ... tert-Amyl chloride; References

  3. 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.

  4. Alkyl group - Wikipedia

    en.wikipedia.org/wiki/Alkyl_group

    Thus, the name is 3-methylpentane to avoid ambiguity: The 3- is because the methyl is attached to the third of the five carbon atoms. If there is more than one of the same alkyl group attached to a chain, then the prefixes are used on the alkyl groups to indicate multiples (i.e., di, tri, tetra, etc.)

  5. tert-Amyl chloride - Wikipedia

    en.wikipedia.org/wiki/Tert-Amyl_chloride

    tert-Amyl chloride (2-methyl-2-butyl chloride) is an alkyl chloride used for flavoring and odorizing. [2] At room temperature, it is a colorless liquid with an unpleasant odor. It is an isomer of 1-chloropentane (n-amyl chloride).

  6. Amyl chloride - Wikipedia

    en.wikipedia.org/wiki/Amyl_chloride

    Amyl chloride may refer to any of the monochlorinated derivatives of the isomers of pentane. They have the molecular formula C 5 H 11 Cl. tert-Amyl chloride; 1-Chloropentane (n-amyl chloride) 2-Chloropentane; 3-Chloropentane; 1-Chloro-3-methylbutane (isoamyl chloride)

  7. C5H11Cl - Wikipedia

    en.wikipedia.org/wiki/C5H11Cl

    tert-Amyl chloride (2-methyl-2-butyl chloride) 1-Chloropentane This page was last edited on 26 August 2022, at 19:59 (UTC). Text is available under the Creative ...

  8. tert-Butyl chloride - Wikipedia

    en.wikipedia.org/wiki/Tert-Butyl_chloride

    tert-Butyl chloride is the organochloride with the formula (CH 3) 3 CCl. It is a colorless, flammable liquid. It is sparingly soluble in water, with a tendency to undergo hydrolysis to the corresponding tert-butyl alcohol. It is produced industrially as a precursor to other organic compounds. [1]

  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.