4063-38-1 Usage
Description
(5-Nitro-2-furanyl)methyl thiocyanate, with the chemical formula C7H5N3O3S, is a yellow crystalline solid that exhibits a faint odor. This chemical compound is recognized for its toxic and irritant properties, which make it a potent agent in various applications.
Used in Pharmaceutical Industry:
(5-Nitro-2-furanyl)methyl thiocyanate is used as a synthetic intermediate for the development of pharmaceuticals. Its unique chemical structure allows it to be a key component in the creation of new drugs, contributing to advancements in medicine.
Used in Agrochemical Industry:
In the agrochemical sector, (5-Nitro-2-furanyl)methyl thiocyanate is utilized as a potent pesticide and insecticide. It is effective in controlling and eliminating certain pests and insects by disrupting their nervous systems, thereby protecting crops and enhancing agricultural productivity.
Safety Note:
Given the hazardous nature of (5-Nitro-2-furanyl)methyl thiocyanate, it is crucial to handle this compound with extreme caution. Adherence to proper safety guidelines and protocols is essential when working with this chemical to minimize risks and ensure the well-being of individuals and the environment.
Check Digit Verification of cas no
The CAS Registry Mumber 4063-38-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,0,6 and 3 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 4063-38:
(6*4)+(5*0)+(4*6)+(3*3)+(2*3)+(1*8)=71
71 % 10 = 1
So 4063-38-1 is a valid CAS Registry Number.
InChI:InChI=1/C6H4N2O3S/c7-4-12-3-5-1-2-6(11-5)8(9)10/h1-2H,3H2
4063-38-1Relevant articles and documents
Radical-Nucleophilic Substitution (SRN1) Reactions: Electron Spin Resonance Studies of Electron-capture Processes. Part 4.1 α-Substituted 2-Methyl-5-nitrofurans
Symons, Martyn C. R.,Bowman, W. Russell
, p. 1133 - 1138 (2007/10/02)
We have probed two steps postulated for the radical-nucleophilic substitution (SRN1) mechanism for α-substituted 2-methyl-5-nitrofurans (O2NFurCH2X) by detecting the intermediates involved using e.s.r. spectroscopy.These two steps are the elect
