306969-61-9

Basic information

• Product Name: C₉H₉F₃N₂O₂
• Synonyms: C₉H₉F₃N₂O₂
• CAS NO: 306969-61-9
• Molecular Weight: 234.178
• Mol File: 306969-61-9.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: C₉H₉F₃N₂O₂(CAS DataBase Reference)
• NIST Chemistry Reference: C₉H₉F₃N₂O₂(306969-61-9)
• EPA Substance Registry System: C₉H₉F₃N₂O₂(306969-61-9)

Safety Data

• Hazardous Substances Data: 306969-61-9(Hazardous Substances Data)

Downstream Products

• 455-19-6 4-Trifluoromethylbenzaldehyde 

Relevant articles and documents

Mechanisms of decomposition of α-hydroxydialkylnitrosamines in aqueous solution

A study of the decomposition of α-hydroxydialkylnitrosamines in aqueous 9% acetonitrile, with an ionic strength of 1 M (NaClO4), at 25 °C is reported. Plots of the logarithm of the buffer-independent rate constant, k(o), against pH are concave up and indicate a three-term rate law for the solvent reaction, including acid (k(H+))-, base (k(OH))-, and pH-independent (k(HOH)) terms. Secondary α-deuterium isotope effects for compound 1a, (N-nitrosomethylamino)-phenylmethanol, are as follows: k(α)(H)/k(α)(D) = 1.12 ± 0.03 and 1.19 ± 0.02 for k(H+) and k(OH), respectively. General acid (k(HA)) and general base (k(A-)) catalysis by more acidic carboxylic acid buffers is also observed. Structure reactivity and other parameters obtained in this study, and their changes with substrate and catalyst structure, permit the assignment of mechanisms for the k(H+), k(OH), k(HA), and k(A-) processes.