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Usage

Uses

Used in Chemical Synthesis:
(1E)-2-chloro-N,N-dimethylethanimidamide is utilized as a reagent or intermediate in various chemical reactions. Its unique structure allows it to participate in a range of organic synthesis processes, facilitating the creation of diverse chemical products.
Used in Pharmaceutical Industry:
In the pharmaceutical sector, (1E)-2-chloro-N,N-dimethylethanimidamide may be employed as a building block for the development of new drugs. Its ability to form stable intermediates can be leveraged to synthesize medicinal compounds with potential therapeutic applications.
Used in Research and Development:
(1E)-2-chloro-N,N-dimethylethanimidamide is also used in research and development settings to explore its chemical properties and potential applications. Scientists can study its reactivity and interactions with other compounds to discover new uses and optimize existing processes.
It is crucial to handle (1E)-2-chloro-N,N-dimethylethanimidamide with care due to its toxic nature. Ingestion or inhalation can lead to adverse health effects, and it can cause skin and eye irritation. Moreover, proper disposal and handling are necessary to mitigate environmental risks associated with (1E)-2-chloro-N,N-dimethylethanimidamide.

Downstream Products

• 105076-16-2 N,N-dimethyl-N'-(p-nitrobenzyloxycarbonyl)chloroacetamidine 
• 121721-52-6 N,N-Dimethyl-N'-(p-toluenesulfonyl)-2-chloroacetamidine 
• 10319-72-9 N,N-Dimethyl-acetamidin-2-thiolsulfat 

Relevant academic research and scientific papers

Phosphoric acid esters, composition and use

Phosphoric (phosphonic) acid esters of the formula STR1 where R1 denotes linear or branched alkyl of up to 4 carbon atoms, R2 denotes linear or branched alkyl, alkoxy or alkylthio, each of up to 4 carbon atoms, mono- or dialkylamino of up to 4 carbon atoms in each alkyl, or phenyl, R3 denotes linear or branched alkoxy or alkylthio of up to 4 carbon atoms, amino, mono- or dialkylamino of up to 4 carbon atoms in each alkyl, alkylalkoxyalkylamino of up to 4 carbon atoms in each alkyl or alkoxyalkyl, dialkoxyalkylamino of up to 4 carbon atoms in each alkoxyalkyl, alkylalkenylamino of up to 4 carbon atoms in each alkyl or alkenyl, alkylalkynylamino of up to 4 carbon atoms in each alkyl or alkynyl, N-methyl-N-methoxyamino, N-(2-methoxyethyl)-N-(2-cyanoethyl), a 5- or 6-membered nitrogenous heterocyclic ring which may contain several nitrogen atoms and optionally oxygen as ring members, R4 denotes unsubstituted or halogen-substituted acyl of up to 4 carbon atoms, alkylsulfonyl or haloalkylsulfonyl of up to 4 carbon atoms in each alkyl or haloalkyl, the group --CO--NR5 R6, R5 and R6 denoting hydrogen, linear or branched alkyl of up to 4 carbon atoms, or - but not simultaneously - phenyl, or R5 and R6 denoting, together with the nitrogen atom whose substituents they are, a 5- or 6-membered heterocyclic ring with further nitrogen atoms and an oxygen atom as ring members, or R4 denotes the group --CO--Y--R7, R7 denoting linear or branched alkyl of up to 4 carbon atoms, phenyl or benzyl, and Y denoting oxygen or sulfur, and X denotes oxygen or sulfur, which are effective against pests, especially insects, mites and ticks; pesticides containing these phosphoric (phosphonic) acid esters as active ingredients; a process for producing these active ingredients; and a process for combating pests with these active ingredients.