TRIS(4-AMINOPHENYL)METHANE

For research use only. Not for therapeutic Use.

  • CAT Number: M000286
  • CAS Number: 548-61-8
  • Molecular Formula: C19H19N3
  • Molecular Weight: 289.38
  • Purity: ≥95%
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Tris(4-aminophenyl)methane(Cat No.:M000286)is a versatile organic compound commonly used in pharmaceutical and chemical research. Featuring three 4-aminophenyl groups attached to a central methane core, it is valuable in the synthesis of various molecular structures. This compound serves as an intermediate in the production of dyes, polymers, and other bioactive molecules. Its aromatic amine groups offer functional versatility, making it useful in drug development and material science. Tris(4-aminophenyl)methane is particularly significant in studies involving electron transfer, aromatic interactions, and molecular design for advanced applications.


Catalog Number M000286
CAS Number 548-61-8
Synonyms

4,4’,4’’-methylidynetri-anilin;4,4’,4’’-methylidynetris-benzeneamin;4,4’,4’’-methylidynetrisbenzeneamine;4,4’,4’’-triaminotriphenylmethane;leucoparafuchsin;leucoparafuchsine;p,p’,p’’-triaminotriphenylmethane;triaminotriphenylmethane

Molecular Formula C19H19N3
Purity ≥95%
Target HCV
Storage RT
IUPAC Name 4-[bis(4-aminophenyl)methyl]aniline
InChI InChI=1S/C19H19N3/c20-16-7-1-13(2-8-16)19(14-3-9-17(21)10-4-14)15-5-11-18(22)12-6-15/h1-12,19H,20-22H2
InChIKey ADUMIBSPEHFSLA-UHFFFAOYSA-N
SMILES C1=CC(=CC=C1C(C2=CC=C(C=C2)N)C3=CC=C(C=C3)N)N
Reference

<span style=”color:#000000;”><span style=”text-decoration: none; line-height: 18px; font-family: Arial, -apple-system, sans-serif; font-variant-ligatures: normal; orphans: 2; text-align: justify; widows: 2;”>1.&nbsp;</span></span><span style=”text-decoration: none; line-height: 18px; font-family: Arial, -apple-system, sans-serif; font-variant-ligatures: normal; orphans: 2; text-align: justify; widows: 2;”><span style=”text-decoration: none; line-height: 18px; font-family: Arial, -apple-system, sans-serif; font-variant-ligatures: normal; orphans: 2; text-align: justify; widows: 2;”><a href=”https://www.ncbi.nlm.nih.gov/pubmed/19419203″ rel=”nofollow” style=”color: rgb(122, 122, 122); text-decoration: none; line-height: 18px; font-family: Arial, -apple-system, sans-serif; font-variant-ligatures: normal; orphans: 2; text-align: justify; widows: 2;” target=”_blank”><span style=”color:#000000;”>Chen CS, et al. Structure-based discovery of triphenylmethane derivatives as inhibitors of hepatitis C virushelicase. J Med Chem. 2009 May 14;52(9):2716-23.</span></a></span><br />
<span style=”color: rgb(0, 0, 0); text-decoration: none; line-height: 18px; font-family: Arial, -apple-system, sans-serif; font-variant-ligatures: normal; orphans: 2; text-align: justify; widows: 2;”>2.<span style=”font-family: Arial, sans-serif; font-size: 13px; font-variant-ligatures: normal;”>Kamme, Fredrik C., et al. &quot;Preservation of RNA in a biological sample.&quot; U.S. Patent No. 7,056,673. 6 Jun. 2006.</span></span></span>

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