113211-44-2 Usage
Uses
Used in Pharmaceutical Research:
3-AMINOXY-1-NITRILEPROPANE HYDROCHOLORIDE is used as a reagent in the synthesis of various organic compounds, particularly in the production of pharmaceuticals. Its versatile reactivity allows for the creation of a wide range of bioactive compounds, making it a valuable component in drug development.
Used in Agrochemical Production:
In the agrochemical industry, 3-AMINOXY-1-NITRILEPROPANE HYDROCHOLORIDE is used as a key intermediate in the synthesis of various agrochemicals. Its unique properties enable the development of effective and targeted agrochemicals for crop protection and pest control.
Used in Organic Synthesis:
3-AMINOXY-1-NITRILEPROPANE HYDROCHOLORIDE is utilized as a reagent in the synthesis of a variety of organic compounds across different industries. Its ability to participate in various chemical reactions makes it a valuable tool in the creation of new and innovative organic compounds.
Used in Fine Chemicals Production:
In the production of fine chemicals, 3-AMINOXY-1-NITRILEPROPANE HYDROCHOLORIDE is employed as an intermediate due to its unique structure and reactivity. Its involvement in the synthesis process contributes to the development of high-quality and specialized fine chemicals for various applications.
Check Digit Verification of cas no
The CAS Registry Mumber 113211-44-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,3,2,1 and 1 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 113211-44:
(8*1)+(7*1)+(6*3)+(5*2)+(4*1)+(3*1)+(2*4)+(1*4)=62
62 % 10 = 2
So 113211-44-2 is a valid CAS Registry Number.
113211-44-2Relevant academic research and scientific papers
Symmetrical O-substituted dioximes of benzo-fused β-diketocyclo-alkylenes, the processes for their preparation and their application as drugs
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, (2008/06/13)
Drugs with high anticonvulsant and analgesic activities constituted by symmetrical β-dialkoxyiminocycloalklene derivatives in which the imine double bonds are conjugated with the cyclic double bond or bonds belonging to one or more fused benzene rings. They correspond to the general formula I: STR1
