Indol - ορισμός. Τι είναι το Indol
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Τι (ποιος) είναι Indol - ορισμός

CHEMICAL COMPOUND
3,3'-diindolylmethane; Diindolylmethane; 3,3'-methylenebis-1H-indole; 3-(1H-indol-3-ylmethyl)-1H-indole

Indol         
  • Baeyer's original structure for indole, 1869
  • 2-position lithiation of indole
  • The Fischer indole synthesis
  • Synthesis of gramine from indole
  • center
  • Example of a cycloaddition of indole
  • Oxidation of indole by ''N''-bromosuccinimide
  • The Vilsmeyer–Haack formylation of indole
  • Formation and reactions of the indole anion
  • Reaction of [[aniline]] and [[ethylene glycol]] to give indole.
  • The Leimgruber–Batcho indole synthesis
  • One-pot microwave-assisted synthesis of indole from phenylhydrazine and pyruvic acid
  • Indole is produced via anthranilate and reacts further to give the amino acid tryptophan.
·noun A white, crystalline substance, C8H7N, obtained from blue indigo, and almost all indigo derivatives, by a process of reduction. It is also formed from albuminous matter, together with skatol, by putrefaction, and by fusion with caustic potash, and is present in human excrement, as well as in the intestinal canal of some herbivora.
indole         
  • Baeyer's original structure for indole, 1869
  • 2-position lithiation of indole
  • The Fischer indole synthesis
  • Synthesis of gramine from indole
  • center
  • Example of a cycloaddition of indole
  • Oxidation of indole by ''N''-bromosuccinimide
  • The Vilsmeyer–Haack formylation of indole
  • Formation and reactions of the indole anion
  • Reaction of [[aniline]] and [[ethylene glycol]] to give indole.
  • The Leimgruber–Batcho indole synthesis
  • One-pot microwave-assisted synthesis of indole from phenylhydrazine and pyruvic acid
  • Indole is produced via anthranilate and reacts further to give the amino acid tryptophan.
['?nd??l]
¦ noun Chemistry a crystalline organic compound with an unpleasant odour, present in coal tar and in faeces.
Origin
C19: blend of indigo (because obtained artificially from indigo blue) and L. oleum 'oil'.
Indoles         
  • Baeyer's original structure for indole, 1869
  • 2-position lithiation of indole
  • The Fischer indole synthesis
  • Synthesis of gramine from indole
  • center
  • Example of a cycloaddition of indole
  • Oxidation of indole by ''N''-bromosuccinimide
  • The Vilsmeyer–Haack formylation of indole
  • Formation and reactions of the indole anion
  • Reaction of [[aniline]] and [[ethylene glycol]] to give indole.
  • The Leimgruber–Batcho indole synthesis
  • One-pot microwave-assisted synthesis of indole from phenylhydrazine and pyruvic acid
  • Indole is produced via anthranilate and reacts further to give the amino acid tryptophan.
·noun Natural disposition; natural quality or abilities.

Βικιπαίδεια

3,3'-Diindolylmethane

3,3′-Diindolylmethane (DIM) is a compound derived from the digestion of indole-3-carbinol, found in cruciferous vegetables, such as broccoli, Brussels sprouts, cabbage and kale. It and its parent compound – indole-3-carbinol – are under laboratory research to determine their possible biological properties, particularly in anti-cancer mechanisms. DIM is sold as a dietary supplement.