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CAS 52664-35-4

:

Phenol, 4-amino-, 1,1′,1′′-phosphorothioate

Description:
Phenol, 4-amino-, 1,1′,1′′-phosphorothioate, commonly referred to as a phosphorothioate compound, is characterized by its unique chemical structure that includes a phenolic group, an amino group, and a phosphorothioate moiety. This compound typically exhibits properties associated with both phenols and organophosphorus compounds, such as moderate solubility in organic solvents and potential reactivity with nucleophiles due to the presence of the phosphorothioate group. It may also display biological activity, which can include herbicidal or insecticidal properties, making it of interest in agricultural chemistry. The amino group can participate in hydrogen bonding, influencing its interactions in biological systems. Additionally, the compound's stability and reactivity can be affected by environmental factors, such as pH and temperature. Safety considerations are essential when handling this substance, as it may pose health risks similar to other organophosphorus compounds. Overall, its unique combination of functional groups contributes to its diverse applications and potential effects in various chemical and biological contexts.
Formula:C18H18N3O3PS
InChI:InChI=1/C18H18N3O3PS/c19-13-1-7-16(8-2-13)22-25(26,23-17-9-3-14(20)4-10-17)24-18-11-5-15(21)6-12-18/h1-12H,19-21H2
InChI key:InChIKey=MBUAAMOJATXYKR-UHFFFAOYSA-N
SMILES:P(OC1=CC=C(N)C=C1)(OC2=CC=C(N)C=C2)(OC3=CC=C(N)C=C3)=S
Synonyms:
  • Phenol, p-amino-, O,O,O-triester with phosphorothioic acid
  • Phosphorothioic acid, O,O,O-tris(p-aminophenyl) ester
  • Phenol, 4-amino-, phosphorothioate (3:1) (ester)
  • Tris(4-aminophenyl) phosphorothioate
  • TPTA
  • O,O,O-tris(4-aminophenyl) phosphorothioate
  • Phenol, 4-amino-, 1,1′,1′′-phosphorothioate
  • Thionophosphoric acid-tris-(p-aminophenyl ester)
  • Tris(4-Amino Phenyl)thiophos
  • Einecs 258-083-6
  • See more synonyms
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