92075-16-6

Usage

Uses

Used in Coatings Industry:
1-TERT-BUTYL-2-IMIDAZOLIDINONE is used as a solvent for enhancing the performance and quality of coatings. Its high solvency power allows for better dissolution of coating components, leading to improved adhesion, durability, and finish.
Used in Adhesives Industry:
In the adhesives industry, 1-TERT-BUTYL-2-IMIDAZOLIDINONE serves as a solvent, improving the adhesive's bonding strength and flexibility. Its properties contribute to the formulation of adhesives that offer strong, long-lasting bonds with a wide range of materials.
Used in Inks Industry:
1-TERT-BUTYL-2-IMIDAZOLIDINONE is utilized as a solvent in ink formulations, providing a consistent flow and even distribution of color. Its use results in inks with vibrant colors, sharp image quality, and resistance to fading.
Used as a Reaction Medium:
1-TERT-BUTYL-2-IMIDAZOLIDINONE is employed as a reaction medium in various chemical processes. Its ability to dissolve a wide range of substances makes it suitable for facilitating numerous types of chemical reactions, thus improving the efficiency and yield of these processes.
Used as a Dispersing Agent in Dyes and Pigments:
In the formulation of dyes and pigments, 1-TERT-BUTYL-2-IMIDAZOLIDINONE acts as a dispersing agent. It helps in evenly distributing the colorants throughout the medium, ensuring a uniform appearance and preventing the settling of pigments.

InChI:InChI=1/C7H14N2O/c1-7(2,3)9-5-4-8-6(9)10/h4-5H2,1-3H3,(H,8,10)

Upstream product

• 120-93-4 imidazolidone 
• 75-65-0 tert-butyl alcohol 
• 1943-83-5 2-chloroethyl isothiocyanate 
• 75-64-9 tert-butylamine 
• 92075-17-7 1-tert-butyl-1,3-dihydro-2H-imidazol-2-one 
• 13908-02-6 1-(tert-butyl)-3-(2-chloroethyl)urea 

Downstream Products

• 1040130-04-8 1-tert-butyl-3-[4-(methylsulfanyl)phenyl]imidazolidin-2-one 
• 1325189-12-5 1-tert-butyl-3-(4-methoxy-3-(4-methylpiperazin-1-yl)phenyl)imidazolidin-2-one 
• 1325189-94-3 C₁₄H₂₁N₃O₂ 
• 1325189-91-0 C₁₄H₁₉N₃O₄ 
• 1238698-48-0 1-[4-(3-tert-butyl-2-oxoimidazolidin-1-yl)-2-fluorophenyl]-5-methoxy-3-(1-phenyl-1H-pyrazol-5-yl)pyridazin-4(1H)-one 

Relevant academic research and scientific papers

Synthesis and structural characterization of tris(2-oxo-1-tert- butylimidazolyl) and tris(2-oxo-1-methylbenzimidazolyl)hydroborato complexes: A new class of tripodal oxygen donor ligand

A new class of tripodal L2X ligands that feature three oxygen donors, namely the tris(2-oxo-1-tert-butylimidazolyl) and tris(2-oxo-1- methylbenzimidazolyl)hydroborato ligands, [To But] and [To MeBenz], has been synthesized via the reactions of NaBH4 with the respective imidazolone. Structural and spectroscopic studies indicate that both [To But] and [ToMeBenz] are significantly more sterically demanding but less electron donating than the related [O3] donor ligand, [CpCo{P(O)(OEt)2}3].

Cyclic Ureate Tantalum Catalyst for Preferential Hydroaminoalkylation with Aliphatic Amines: Mechanistic Insights into Substrate Controlled Reactivity

The efficient and catalytic amination of unactivated alkenes with simple secondary alkyl amines is preferentially achieved. A sterically accessible, N,O-chelated cyclic ureate tantalum catalyst was prepared and characterized by X-ray crystallography. This

GROUP 5 METAL COMPLEXES FOR PRODUCING AMINE-FUNTIONALIZED POLYOLEFINS

This application pertains to group 5 metal complexes having the structure of Formula I: and their potential utility in catalyzing amination of polyolefins having alkene groups.amine-

GROUP 5 METAL COMPLEXES FOR CATALYTIC AMINE FUNCTIONALIZATION

This application pertains to group 5 metal complexes having the structure of Formula I; and their potential utility in catalyzing α-alkylation of secondary amine-containing moieties.

IMIDAZOLIDINONES AND ANALOGS EXHIBITING ANTI-CANCER AND ANTI-PROLIFERATIVE ACTIVITIES

Described are compounds of Formula I which find utility in the treatment of cancer, autoimmune diseases and metabolic bone disorders through inhibition of c-FMS (CSF-1R), c-KIT, and/or PDGFR kinases. These compounds also find utility in the treatment of other mammalian diseases mediated by c-FMS, c-KIT, or PDGFR kinases.

Linear and macrocyclic ligands containing alternating pyridine and imidazolidin-2-one units

Linear oligomers of alternating 2,6-disubstituted pyridine (P) and N,N′-disubstituted imidazolidine-2-one (I) units have been made rapidly and in high yield with up to nine repeating units, terminating in either pyridine or imidazolidin-2-one units, or one of each. Synthetic methods include: (1) the sodium hydride-mediated condensation of N-(tert-butyl)imidazolidin-2-one with 2,6-difluoropyridine (F-P-F) or with higher analogues such as F-PIP-F, to give IPI, IPIPI and IPIPIPI. (The tert-butyl protection is readily and quantitatively removed with acid.) (2) The caesium fluoride catalysed interaction of N,N′-[dimethyl(1,1,3-trimethylpropyl)]-protected IPI with But-IP-F sequentially leads firstly to IPIPIPI which by the same method reacts with F-P-F to give F-PIPIPIPIP-F. (3) F-P-F also reacts with 1,2-ethylenediamine (E) sequentially to give F-PEP-F, EPEPE and F-PEPEPEP-F while similar reactions starting from F-PIP-F give EPIPE and F-PEPIPEP-F in sequence. Alternative routes examined include: (1) the interaction of F-P-F with imidazole to give 2,6-bis(imidazol-1-yl)pyridine and salts therefrom followed by (unsuccessful) oxidation. (2) The reaction of 2,6-diaminopyridine with 2-chloroethyl isocyanate followed by cyclisation to give IPI. (3) The interaction of 2,6-diaminopyridine with oxalate esters (O) to give OPO or H2N-POP-NH2, the latter of which was reduced to H2N-PEP-NH2. Cyclisation of the linear assemblies was not successful. However macrocyclic systems were made by linking two IPI units with two ethoxyethyl or with two ethoxyethoxyethyl units. Also two F-PIP-F units were similarly reacted to give polyether-linked macrocycles. Mono- and bis-prop-2-ynylated IPI derivatives were made but could not be cyclised. Attempts to cyclise ethylenediamine and oxamide based systems were also unsuccessful. The linear and macrocyclic ligands showed calcium selectivity in a study of their metal complexing abilities.

Photochemical Elimination of Nitrogen from 1-(1-Alkenyl)-4-tert-butyl-1,4-dihydro-5H-tetrazol-5-ones. Competition between Addition of Methanol and Cyclization of a Dipolar Intermediate

The 4-tert-butyl-1-vinyltetrazolones 12a-c and the tetrazolones 13 and 14 are synthesized from the 5-chlorotetrazole 7 and the tetrazolone 9 via several routes.Bis(benzonitrile)palladium dichloride catalyses the O -> N-Claisen rearrangement 8 -> 11, the a