67330-66-9

Upstream product

• 84487-46-7 ortho-(cyclopent-2-en-1-yl)aniline 
• 62-53-3 aniline 
• 142-29-0 cyclopentene 
• 96-41-3 Cyclopentanol 
• 700-88-9 cyclopentylbenzene 
• 91088-21-0 <2,4-Dinitro-phenyl>-cyclopentan 
• 91180-95-9 <4-Amino-2-nitro-phenyl>-cyclopentan 
• 287944-10-9 2-cyclopent-1-enyl-4,4,5,5-tetramethyl-[1,3,2]dioxaborolane 
• 88-73-3 2-Chloronitrobenzene 
• 120-92-3 cyclopentanone 
• 28075-49-2 1-cyclopentenyl triflate 
• 71-43-2 benzene 
• 96-40-2 2-cyclopenten-1-yl chloride 
• 609-73-4 o-nitroiodobenzene 

Downstream Products

• 1373752-01-2 1-azido-2-cyclopentylbenzene 
• 1449199-65-8 N-(2-cyclopentylphenyl)hydrazinecarbothioamide 
• 1449199-66-9 (E)-N-(2-cyclopentylphenyl)-2-(4-(1-(4-(trifluoromethoxy)phenyl)-1H-1,2,4-triazol-3-yl)benzylidene)hydrazinecarbothioamide 
• 1449199-89-6 1-cyclopentyl-2-isothiocyanatobenzene 
• 942913-83-9 N-(4-cyclopentylphenyl)-2-(3-methyl-2,6-dioxo-1,2,3,6-tetrahydropurin-7-yl)acetamide 
• 1072933-96-0 2-[(2-cyclopentylphenylimino)methyl]phenol 
• 1072934-09-8 2-tert-butyl-6-[(2-cyclopentylphenylimino)methyl]phenol 
• 1072934-20-3 4,6-di-tert-butyl-2-[(2-cyclopentylphenylimino)methyl]phenol 

Relevant academic research and scientific papers

PESTICIDAL COMPOSITIONS AND PROCESSES RELATED THERETO

This document discloses molecules having the following formulas (“Formula One” and“Formula Two” and “Formula Three”) The Ar1, Het, Ar2, R1, R2, R3, R4, and R5 are further described herein.

PESTICIDAL COMPOSITIONS AND PROCESSES RELATED THERETO

This document discloses molecules having the following formulas (“Formula One” and“Formula Two” and “Formula Three”) The Ar1, Het, Ar2, R1, R2, R3, R4, and R5 are further described herein.

Rh2(II)-catalyzed intramolecular aliphatic C-H bond amination reactions using aryl azides as the N-atom source

Rhodium(II) dicarboxylate complexes were discovered to catalyze the intramolecular amination of unactivated primary, secondary, or tertiary aliphatic C-H bonds using aryl azides as the N-atom precursor. While a strong electron-withdrawing group on the nitrogen atom is typically required to achieve this reaction, we found that both electron-rich and electron-poor aryl azides are efficient sources for the metal nitrene reactive intermediate.

Methods and compositions for treating pain

The present application relates to compounds and methods for treating pain, incontinence and other conditions.

Proton-catalyzed hydroamination and hydroarylation reactions of anilines and alkenes: A dramatic effect of counteranions on reaction efficiency

The anilinium salt, [PhNH3][B(C6F5)4], has been identified as a catalyst for the hydroamination and hydroarylation of several different types of alkenes with anilines. The weakly coordinating counterion of this

Design of arylimine postmetallocene catalytic systems for olefin polymerization: I. Synthesis of substituted 2-cycloalkyl- and 2,6-dicycloalkylanilines

A convenient synthetic approach to substituted 2-cycloalkyl- and 2,6-dicycloalkylanilines, involving catalytic hydrogenation on Raney nickel in methanol of readily available o-cycloalkenylanilines prepared by reaction of cyclic alkyl halides with anilines