31180-79-7

Usage

Uses

Used in Pharmaceutical Industry:
(2E)-1,7,7-trimethyl-N-nitrobicyclo[2.2.1]heptan-2-imine serves as a key intermediate in the synthesis of various pharmaceuticals, leveraging its reactive functional groups to form a wide range of bioactive compounds.
Used in Agrochemical Industry:
(2E)-1,7,7-trimethyl-N-nitrobicyclo[2.2.1]heptan-2-imine is utilized as a precursor in the development of agrochemicals, contributing to the creation of effective products for agricultural applications.
Used in Organic Chemistry Research:
(2E)-1,7,7-trimethyl-N-nitrobicyclo[2.2.1]heptan-2-imine is employed as a building block in organic chemistry for the synthesis of complex organic compounds, exploring its potential in forming various derivatives with different functional groups.

Upstream product

• 13559-66-5 (+/-)-camphor oxime 
• 67-66-3 chloroform 
• 2792-42-9 (R,R)-camphor oxime 
• 7697-37-2 nitric acid 
• 18674-50-5 camphor oxime 
• 76-22-2 Camphor 
• 2792-42-9 camphor oxime 
• 736109-58-3 1,7,7-trimethyl-bicyclo[2.2.1]heptan-2-one 
• 60-29-7 diethyl ether 
• 7782-77-6 cis-nitrous acid 
• 64-19-7 acetic acid 
• 7647-01-0 hydrogenchloride 

Downstream Products

• 508-32-7 1,7,7-trimethyltricyclo[2.2.1.02,6]heptane 
• 79-92-5 camphene 
• 287488-25-9 (1R,4R)-1,7,7-trimethylbicyclo[2.2.1]heptan-2-imine 
• 7519-74-6 thiocamphor 
• 10281-41-1 camphor semicarbazone 

Relevant academic research and scientific papers

AMINATION AND HYDROXYLATION OF ARYLMETAL COMPOUNDS

In one aspect, the present disclosure provides methods of preparing a primary or secondary amine and hydroxylated aromatic compounds. In some embodiments, the aromatic compound may be unsubstituted, substituted, or contain one or more heteroatoms within the rings of the aromatic compound. The methods described herein may be carried out without the need for transition metal catalysts or harsh reaction conditions.

Urea activation of nitrimines: A mild, metal-free approach to sterically hindered enamines

Nitrimines have been identified as impressive starting points for the syntheses of otherwise inaccessible, sterically encumbered enamines. The activation of nitrimines with urea catalysts for reaction with a variety of amines enables the formation of high

ON THE FORMATION AND NITROGEN NUCLEAR MAGNETIC RESONANCE SPECTRA OF SOME NITRIMINES ('PERNITROSO-KETONES'), AND THE MECHANISM OF OXIME CLEAVAGE BY NITROUS ACID

The formation of nitrimines, by the action of nitrous acid in oximes, is shown to proceed without scrambling of the nitrogen atoms, the oxime nitrogen forming the imine, and the nitrous acid generating the nitro group.Colorued intermediates in the reaction are proposed to be nitrosimines.The mechanism of nitrosative deoximation, and the nitrogen NMR spectra of nitrimines, are reported and discussed.