56962-16-4 Usage
Uses
Used in Chemical Synthesis Industry:
2,3,4,5-Tetrachlorobenzaldehyde is used as a chemical intermediate for the production of dyes, which are essential for coloring textiles, plastics, and other materials. Its unique structure allows for the creation of a wide range of colorants with specific properties.
Used in Pharmaceutical Industry:
In the pharmaceutical sector, 2,3,4,5-Tetrachlorobenzaldehyde is utilized as a precursor in the synthesis of various medicinal compounds. Its chemical reactivity and structural features make it a valuable component in the development of new drugs with specific therapeutic targets.
Used in Pesticide Production:
2,3,4,5-Tetrachlorobenzaldehyde is employed as a key intermediate in the manufacturing process of certain pesticides. Its chemical properties contribute to the effectiveness of these products in controlling pests and protecting crops.
Check Digit Verification of cas no
The CAS Registry Mumber 56962-16-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,9,6 and 2 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 56962-16:
(7*5)+(6*6)+(5*9)+(4*6)+(3*2)+(2*1)+(1*6)=154
154 % 10 = 4
So 56962-16-4 is a valid CAS Registry Number.
56962-16-4Relevant academic research and scientific papers
The cheletropic ene-reaction and its reversal; additions to 1,2,3,4-tetrachloro-5-methylenecyclohexa-1,3-diene
Grimme, Wolfram,Haerter, Michael W.,Sklorz, Christoph A.
, p. 1959 - 1966 (2007/10/03)
The cheletropic ene-reaction is presented as an extension of the known pericyclic additions. No example of this process is known but some decarbonylations have been discussed as its reverse. The scope of these reactions is extended by the facile decarbonylation of the alicyclic trienal 11 to give o-xylene. The dramatic lowering of the activation energy when an arene is formed and the finding that in this system phenyl isocyanide can also act as a chelefuge underline the pericyclic character of this reaction. In quest of a cheletropic addition to an ene 1,2,3,4-tetrachloro-5-methylenecyclohexa-1,3-diene was reacted with CO under pressure but to no avail. The reactive ene however readily adds an electron deficient ketone and molecular oxygen.
