7510-10-3 Usage
Uses
Used in Pharmaceutical Production:
2,4,6-trichlorophenyl 4-nitrobenzoate is utilized as an intermediate in the production of pharmaceuticals. Its unique chemical structure allows it to be a key component in the synthesis of various medicinal compounds, contributing to the development of new drugs and therapies.
Used in Agrochemical Synthesis:
In the agrochemical industry, 2,4,6-trichlorophenyl 4-nitrobenzoate serves as an intermediate for the synthesis of various agrochemicals. Its application aids in the development of pesticides, herbicides, and other agricultural products that are essential for crop protection and yield enhancement.
Used in Organic Compound Synthesis:
2,4,6-trichlorophenyl 4-nitrobenzoate is also employed in the synthesis of organic compounds. Its versatile chemical properties make it a valuable reagent in various chemical reactions, facilitating the creation of a wide range of organic molecules for different applications.
Used as a Chemical Reaction Reagent:
Due to its reactivity and functional groups, 2,4,6-trichlorophenyl 4-nitrobenzoate is used as a reagent in chemical reactions. It plays a crucial role in facilitating specific transformations and processes, enabling the synthesis of desired products in the fields of organic chemistry and materials science.
Check Digit Verification of cas no
The CAS Registry Mumber 7510-10-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,5,1 and 0 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 7510-10:
(6*7)+(5*5)+(4*1)+(3*0)+(2*1)+(1*0)=73
73 % 10 = 3
So 7510-10-3 is a valid CAS Registry Number.
7510-10-3Relevant academic research and scientific papers
Palladium-catalyzed external-CO-free carbonylation of aryl bromides using 2,4,6-trichlorophenyl formate
Konishi, Hideyuki,Sekino, Tomoyuki,Manabe, Kei
, p. 562 - 567 (2018/05/07)
A practical Pd-catalyzed carbonylation of (hetero)aryl bromides using a crystalline carbon monoxide (CO) surrogate, 2,4,6-trichlorophenyl formate (TCPF), was developed. This reaction proceeds without the slow addition technique that was previously required and with a low catalyst loading (1mol%). The utility of this Pd-catalyzed external-CO-free carbonylation using TCPF was demonstrated in the synthesis of a histone deacetylase inhibitor.
