51581-32-9 Usage
Uses
Used in Pharmaceutical Applications:
3-Pyridyl dimethylcarbamate is used as a reagent in chemical reactions for the synthesis of various pharmaceutical compounds. Its presence in the structure of the compound allows for the development of new drugs with potential therapeutic applications.
Used in Agrochemical Applications:
3-Pyridyl dimethylcarbamate is used as a reagent in the synthesis of agrochemicals, such as pesticides and herbicides. The pyridine ring in its structure contributes to the effectiveness of these products in controlling pests and weeds in agricultural settings.
Used in Organic Synthesis:
3-Pyridyl dimethylcarbamate is used as a reagent in organic synthesis for the preparation of a wide range of organic compounds. Its stability and reactivity make it a valuable component in the synthesis of various chemical products.
Safety Measures:
Due to the potential risks associated with handling 3-Pyridyl dimethylcarbamate, it is essential to take appropriate safety measures. Exposure should be minimized, and proper protective equipment should be used when working with 3-Pyridyl dimethylcarbamate to ensure the safety of individuals and the environment.
Check Digit Verification of cas no
The CAS Registry Mumber 51581-32-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,5,8 and 1 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 51581-32:
(7*5)+(6*1)+(5*5)+(4*8)+(3*1)+(2*3)+(1*2)=109
109 % 10 = 9
So 51581-32-9 is a valid CAS Registry Number.
InChI:InChI=1/C8H10N2O2/c1-10(2)8(11)12-7-4-3-5-9-6-7/h3-6H,1-2H3
51581-32-9Relevant academic research and scientific papers
Determination of the Structure of Products of the Reduction of Pyridostigmine with NaBH4
Horstmann, Volker,Haefelinger, Guenter
, p. 1401 - 1408 (2007/10/02)
The chemical structure of 5 different products of pyridostigmine obtained by reduction with NaBH4 was determined by GC - MS and subsequently confirmed by means of 1H and 13C NMR spectroscopy.Reaction conditions leading almost exclusively to the main product: 3--1-methyl-1,2,5,6-tetrahydropyridine (4) have been determined. - Key words: Pyridostigmine, 3--1-methylpyridiniumbromide, Reduction Products, 1H NMR Spectra, 13C NMR Spectra
