How Do You Spell FLAVANTHRENE?

Pronunciation: [flˈavanθɹˌiːn] (IPA)

Flavanthrene, pronounced as /ˌflævænˈθriːn/, is a chemical compound that consists of two fused aromatic rings. Its spelling can be broken down as "flav-" which refers to its flavonoid component, and "-anthrene" which refers to its anthracene component. The "a" in "flav-" is pronounced as /æ/ and the "e" in "-anthrene" is pronounced as /iː/. The correct spelling and pronunciation of this word is crucial in the field of organic chemistry research.

FLAVANTHRENE Meaning and Definition

  1. Flavanthrene is a chemical compound that belongs to the class of polycyclic aromatic hydrocarbons (PAHs). It is composed of three fused aromatic rings: a benzene ring and two naphthalene rings. Its structure can be described as a linear fusion of a benzene ring onto a naphthalene structure. Flavanthrene has the empirical formula C18H12 and a molecular weight of 228.29 g/mol.

    Flavanthrene is a solid substance that occurs naturally in coal tar, crude oil, and various fossil fuels. It can also be synthetically derived by organic synthesis methods. In terms of its physical properties, flavanthrene appears as dark-colored crystals or powder, exhibiting poor solubility in water but good solubility in organic solvents such as benzene, toluene, and ethanol.

    Due to its polycyclic aromatic structure, flavanthrene exhibits unique chemical and physical properties. It is highly stable and possesses high resistance to oxidation, making it useful in various chemical reactions and industrial applications. Flavanthrene is commonly employed as a starting material or intermediate in organic synthesis, particularly in the production of dyes, pigments, and other organic compounds. Its ability to absorb ultraviolet (UV) light also makes it useful in ultraviolet blocking agents and sunscreen preparations.

    In conclusion, flavanthrene is a polycyclic aromatic hydrocarbon with a linear fusion of benzene onto a naphthalene structure. It is a crystalline compound that occurs naturally in fossil fuels and can be synthesized through organic chemistry techniques. Its stability, solubility, and UV-absorbing properties make it valuable in various industrial applications, including organic synthesis, dyes, pigments, and sunscreens.

Common Misspellings for FLAVANTHRENE

  • dlavanthrene
  • clavanthrene
  • vlavanthrene
  • glavanthrene
  • tlavanthrene
  • rlavanthrene
  • fkavanthrene
  • fpavanthrene
  • foavanthrene
  • flzvanthrene
  • flsvanthrene
  • flwvanthrene
  • flqvanthrene
  • flacanthrene
  • flabanthrene
  • flaganthrene
  • flafanthrene
  • flavznthrene
  • flavsnthrene
  • flavwnthrene

Etymology of FLAVANTHRENE

The word "flavanthrene" is derived from a combination of two terms: "flavan" and "threne".

The term "flavan" refers to a class of organic compounds called flavonoids. Flavonoids are a diverse group of plant metabolites and are well-known for their wide range of biological activities. They play a significant role in many physiological processes, including plant pigmentation, UV filtration, and antioxidant functions.

The suffix "-threne" is commonly used in organic chemistry to denote a polycyclic aromatic hydrocarbon (PAH) compound containing three fused benzene rings. Examples of such compounds include anthracene and phenanthrene.

By combining the term "flavan" with the suffix "-threne", the word "flavanthrene" is formed to describe a polycyclic aromatic compound that contains the characteristic flavonoid structure.

Plural form of FLAVANTHRENE is FLAVANTHRENES

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