64218-50-4 Usage
Uses
Used in Pharmaceutical Industry:
2-CHLORO-1-(4,5-DICHLORO-2-THIENYL)ETHAN-1-ONE is used as an intermediate for the synthesis of pharmaceuticals, contributing to the development of new drugs with potential therapeutic benefits. Its unique chemical structure allows for the creation of a wide range of medicinal compounds, enhancing the treatment options for various diseases and conditions.
Used in Agrochemical Industry:
In the agrochemical sector, 2-CHLORO-1-(4,5-DICHLORO-2-THIENYL)ETHAN-1-ONE is utilized as a precursor in the production of agrochemicals, such as pesticides and herbicides. Its role in the synthesis of these compounds helps to improve agricultural productivity and crop protection, ensuring a stable food supply.
Used in Organic Chemistry Research:
2-CHLORO-1-(4,5-DICHLORO-2-THIENYL)ETHAN-1-ONE is also used as a research compound in organic chemistry, enabling scientists to explore new reactions and mechanisms involving chlorinated ketones. This contributes to the advancement of chemical knowledge and the discovery of innovative applications for this class of compounds.
It is important to handle 2-CHLORO-1-(4,5-DICHLORO-2-THIENYL)ETHAN-1-ONE with caution, as it can be harmful if ingested, inhaled, or comes into contact with skin or eyes. Proper safety measures should be taken when working with this compound to avoid any potential hazards.
Check Digit Verification of cas no
The CAS Registry Mumber 64218-50-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,4,2,1 and 8 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 64218-50:
(7*6)+(6*4)+(5*2)+(4*1)+(3*8)+(2*5)+(1*0)=114
114 % 10 = 4
So 64218-50-4 is a valid CAS Registry Number.
InChI:InChI=1/C6H3Cl3OS/c7-2-4(10)5-1-3(8)6(9)11-5/h1H,2H2
64218-50-4Relevant articles and documents
Bromothiophene Reactions. II. A Novel Rearrangement in the Zinc and Acetic Acid Reduction
Alvares-Insua, A. S.,Conde, S.,Corral, C.
, p. 713 - 716 (2007/10/02)
The elimination of the α-bromine atoms of the bromothienylethanolamine derivatives 2a, b, c, d with zinc and acetic acid unexpectedly involved a migration of the ethanolamine side chain from the 3 to the 2 position in the thiophene ring.Experiments carried out with simpler analogous compounds 3, 4 and 6 seem to indicate that this rearrangement takes place only in those cases in which the carbon atom of the side chain next to the ring supports an oxygen atom capable of being protonated in the reaction medium.A tentative mechanism is proposed to explain the experimental results.
C:Corrosive;
