459200-98-7

Basic information

• Product Name: 1-[3,5-bis(trifluoromethyl)phenyl]-3-phenyl-2-thiourea
• Synonyms: 1-[3,5-bis(trifluoromethyl)phenyl]-3-phenyl-2-thiourea
• CAS NO: 459200-98-7
• Molecular Weight: 364.314
• Mol File: 459200-98-7.mol
• Article Data: 9

Chemical Properties

• CAS DataBase Reference: 1-[3,5-bis(trifluoromethyl)phenyl]-3-phenyl-2-thiourea(CAS DataBase Reference)
• NIST Chemistry Reference: 1-[3,5-bis(trifluoromethyl)phenyl]-3-phenyl-2-thiourea(459200-98-7)
• EPA Substance Registry System: 1-[3,5-bis(trifluoromethyl)phenyl]-3-phenyl-2-thiourea(459200-98-7)

Safety Data

• Hazardous Substances Data: 459200-98-7(Hazardous Substances Data)

Upstream product

• 23165-29-9 3,5-bistrifluoromethylphenylisothiocyanate 
• 62-53-3 aniline 

Relevant articles and documents

A copper-templated, bifunctional organocatalyst: A strongly cooperative dynamic system for the aldol reaction

The study of novel metal-templated dynamic organocatalytic systems has led to the identification of CuSO4 as the most efficient template to assemble monofunctional prolinamide- and thiourea-modified pyridine ligands. The structural and electron

Hydrogen-Bond Catalysis of Imine Exchange in Dynamic Covalent Systems

The reversibility of imine bonds has been exploited to great effect in the field of dynamic covalent chemistry, with applications such as preparation of functional systems, dynamic materials, molecular machines, and covalent organic frameworks. However, acid catalysis is commonly needed for efficient equilibration of imine mixtures. Herein, it is demonstrated that hydrogen bond donors such as thioureas and squaramides can catalyze the equilibration of dynamic imine systems under unprecedentedly mild conditions. Catalysis occurs in a range of solvents and in the presence of many sensitive additives, showing moderate to good rate accelerations for both imine metathesis and transimination with amines, hydrazines, and hydroxylamines. Furthermore, the catalyst proved simple to immobilize, introducing both reusability and extended control of the equilibration process.

METHODS OF PRODUCING METAL SUFLIDES, METAL SELENIDES, AND METAL SULFIDES/SELENIDES HAVING CONTROLLED ARCHITECTURES USING KINETIC CONTROL

The present invention is directed to methods of preparing metal sulfide, metal selenide, or metal sulfide/selenide nanoparticles and the products derived therefrom. In various embodiments, the nanoparticles are derived from the reaction between precursor metal salts and certain sulfur- and/or selenium-containing precursors each independently having a structure of Formula (I), (II), or (III), or an isomer, salt, or tautomer thereof, where Q1,Q2,Q3,R1,R2,R3,R5, and X are defined within the specification.