75647-90-4

Usage

Uses

Used in Pharmaceutical Industry:
Cyclopropyl methoxylamine is used as a chemical intermediate for the synthesis of various pharmaceutical compounds. Its unique structure allows it to be a key component in the development of new drugs, particularly in the area of medicinal chemistry.
Used in Research and Development:
In the field of scientific research, cyclopropyl methoxylamine is used as a reagent in various chemical reactions and experiments. Its distinct properties make it a valuable tool for understanding the behavior of amines and their potential applications in different chemical processes.
Used in Chemical Synthesis:
Cyclopropyl methoxylamine is employed as a building block in the synthesis of more complex organic molecules. Its cyclopropyl and methoxy groups can be used to create a wide range of compounds with diverse applications in various industries, including materials science and specialty chemicals.

InChI:InChI=1/C4H9NO.ClH/c5-6-3-4-1-2-4;/h4H,1-3,5H2;1H

Upstream product

• 2516-33-8 Cyclopropylmethanol 
• 113211-15-7 2-(cyclopropylmethoxy)isoindoline-1,3-dione 

Downstream Products

• 212631-61-3 N-cyclopropylmethoxy-3,4,5-trifluoro-2-(4-iodo-2-methyl-phenylamino)-benzamide 
• 880472-88-8 C₁₄H₁₆ClF₃N₂O₃S 
• 880472-79-7 N-[4-chloro-2-(1-cyclopropylmethoxyiminoethyl)phenyl]trifluoromethanesulfonamide 
• 1193487-32-9 7-(4-bromo-2-fluoro-phenylamino)-5-oxo-1,2,3,5-tetrahydro-indolizine-8-carboxylic acid cyclopropyl-methoxy-amide 
• 1193488-83-3 5-(4-bromo-2-fluoro-phenylamino)-2,2-dimethyl-7-oxo-3a,7,8,8a-tetrahydro-1,3-dioxa-7a-aza-cyclopenta[a]indene-4-carboxylic acid cyclopropylmethoxy-amide 
• 1393352-42-5 (E)-1-{3-[3-(1-methyl-1H-pyrazol-4-yl)quinolin-6-ylmethyl][1,2,4]triazolo[4,3-b]pyridazin-6-yl}ethanone O-cyclopropylmethyloxime 
• 1367283-00-8 (E/Z)-N-(2-((cyclopropylmethoxy)imino)ethyl)-4-(5-(3,5-dichloro-4-fluorophenyl)-5-(trifluoromethyl)-4,5-dihydroisoxazol-3-yl)-1-naphthamide 

Relevant academic research and scientific papers

O-Isocyanates as Uncharged 1,3-Dipole Equivalents in [3+2] Cycloadditions

1,3-Dipoles are commonly used in [3+2] cycloadditions, whereas isoelectronic uncharged dipole variants remain underdeveloped. In contrast to conventional 1,3-dipoles, uncharged dipole equivalents form zwitterionic cycloadducts, which can be exploited to build further molecular complexity. In this work, the first cycloadditions of oxygen-substituted isocyanates (O-isocyanates) were studied experimentally and by DFT calculations. This unique cycloaddition strategy provides access to a novel class of heterocycle aza-oxonium ylides through intramolecular and intermolecular cycloadditions with alkenes. This allowed a systematic study of the reactivity of the transient aza-oxonium ylide intermediate, which can undergo N?O bond cleavage followed by nitrene C?H insertion, and the formation of β-lactams or isoxazolidinones upon varying the structure of the alkene or O-isocyanate reagents.

PROCESS FOR THE PREPARATION OF QUINOLONE BASED COMPOUNDS

The present invention relates to an improved process for the preparation of quinolone based compounds of general formula (I) using intermediate compound of general formula (XII). Invention also provides an improved process for the preparation of compound of formula (I-a) using intermediate compound of formula (XII-a) and some novel impurities generated during process. Compounds prepared using this process can be used to treat anemia.

HETEROCYCLIC OXIME COMPOUNDS

The invention relates to compounds of formula (I) and salts thereof wherein the substituents are as defined in the specification; a compound of formula (I) for use in the treatment of the human or animal body, in particular with regard to c-Met tyrosine kinase mediated diseases or conditions; the use of a compound of formula (I) for manufacturing a medicament for the treatment of such diseases; pharmaceutical compositions comprising a compound of the formula (I), optionally in the presence of a combination partner, and processes for the preparation of a compound of formula (I).

N-ALKOXYAMIDES OF 6-(TRISUBSTITUTED PHENYL)-4-AMINOPICOLINATES AND THEIR USE AS SELECTIVE HERBICIDES FOR CROPS

N-Alkoxyamides of 4-aminopicolinic acids and 6-amino-4-pyrimidinecarboxylates are selective herbicides for corn, canola and sugar beet.

Design, synthesis, bioactivity, and structure-activity relationship (SAR) studies of novel benzoylphenylureas containing oxime ether group

Novel benzoylphenylureas containing an oxime ether group were designed and synthesized by four schemes. These benzoylphenylureas were identified by 1H NMR spectroscopy and element analysis (or HRMS). The bioactivities of the new compounds were evaluated. These benzoylphenylureas exhibited excellent larvicidal activities against oriental armyworm, some of which were much better in comparison with the commercial Flucycloxuron. In particular, the larvicidal activities against oriental armyworm of compounds 1 and 23 were 5-10 times better than that of Flucycloxuron. Most of these benzoylphenyureas exhibited excellent larvicidal activities against mosquito. At the same time, some of these compounds have good plant growth regulatory activities as well.

Parasiticidal 2-alkoxy- and 2-aryloxyiminoalkyl trifluoromethanesulfonanilides

A series of novel 2-alkoxy- and 2-aryloxyiminoalkyl trifluoromethanesulfonanilide derivatives have shown significant in vitro parasiticidal activity against the ectoparasites Ctenocephalides felis and Rhipicephalus sanguineus. A number of these compounds also displayed significant in vitro endoparasite activity against the nematode Haemonchus contortus. Crown Copyright