10351-06-1 Usage
Uses
Used in Chemical Synthesis:
2,3,5,6-Tetrachloropyridine-4-thiol is used as a reagent in chemical synthesis for its ability to participate in various organic reactions, contributing to the formation of new compounds with desired properties.
Used in Agrochemical Production:
In the agrochemical industry, 2,3,5,6-Tetrachloropyridine-4-thiol is utilized as an intermediate in the production of various agrochemicals, playing a crucial role in the development of effective pesticides and other agricultural products.
Used in Pharmaceutical Production:
Similarly, in the pharmaceutical sector, 2,3,5,6-Tetrachloropyridine-4-thiol serves as an intermediate, aiding in the synthesis of different medicinal compounds, thus contributing to the development of new drugs and therapies.
Safety and Handling:
Given its toxic and hazardous nature, 2,3,5,6-Tetrachloropyridine-4-thiol requires careful handling and proper storage to ensure the safety of human health and the environment. Adequate measures should be taken to minimize exposure and potential risks associated with this chemical compound.
Check Digit Verification of cas no
The CAS Registry Mumber 10351-06-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,3,5 and 1 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 10351-06:
(7*1)+(6*0)+(5*3)+(4*5)+(3*1)+(2*0)+(1*6)=51
51 % 10 = 1
So 10351-06-1 is a valid CAS Registry Number.
InChI:InChI=1/C5HCl4NS/c6-1-3(11)2(7)5(9)10-4(1)8/h(H,10,11)
10351-06-1Relevant articles and documents
REACTION OF POLYHALOPYRIDINES. 5. REACTION OF 2,3,5,6-TETRACHLORO-4-TRIFLUOROMETHYLTHIOPYRIDINE WITH NUCLEOPHILIC REAGENTS
Sipyagin, A. M.,Pal'tsun, S. V.,Pomytkin, I. A.,Aleinikov, N. N.
, p. 56 - 59 (2007/10/02)
The reaction on 2,3,5,6-tetrachloro-4-trifluoromethylthiopyridine with various nucleophilic reagents has been studied.It was shown that CF3S group is readily replaced under the action of O- and S-nucleophiles.Competition was detected between replacement of an α-chlorine atom on the pyridine ring and of the fluorine-containing group under the action of N-nucleophilic reagents.New derivatives of trichlorotrifluoromethylthiopyridine with nitrogen-containing substituents have been synthesized.
