737797-16-9 Usage
Uses
Used in Pharmaceutical Synthesis:
2,4-DICHLOROBENZYLZINC CHLORIDE is used as a synthetic reagent for the preparation of pharmaceuticals and other organic compounds. Its ability to react with a wide range of functional groups allows for the efficient synthesis of complex organic molecules, contributing to the development of new drugs and therapeutic agents.
Used in Organic Reactions as a Catalyst:
In the field of organic chemistry, 2,4-DICHLOROBENZYLZINC CHLORIDE is utilized as a catalyst to facilitate various organic reactions. Its role in the formation of carbon-carbon and carbon-heteroatom bonds is particularly significant, enabling chemists to achieve desired outcomes more efficiently and with greater selectivity.
Used in the Preparation of Complex Organic Molecules:
2,4-DICHLOROBENZYLZINC CHLORIDE is employed as a key reagent in the synthesis of complex organic molecules. Its versatility in reacting with different functional groups makes it an indispensable tool for chemists working on the development of novel organic compounds with potential applications in various industries, including pharmaceuticals, materials science, and agrochemicals.
Check Digit Verification of cas no
The CAS Registry Mumber 737797-16-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,3,7,7,9 and 7 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 737797-16:
(8*7)+(7*3)+(6*7)+(5*7)+(4*9)+(3*7)+(2*1)+(1*6)=219
219 % 10 = 9
So 737797-16-9 is a valid CAS Registry Number.
InChI:InChI=1/C7H5Cl2.ClH.Zn/c1-5-2-3-6(8)4-7(5)9;;/h2-4H,1H2;1H;/q;;+1/p-1/rC7H5Cl3Zn/c8-6-2-1-5(4-11-10)7(9)3-6/h1-3H,4H2
737797-16-9Relevant academic research and scientific papers
Coutant, Eloi P.,Janin, Yves L.
, p. 511 - 516 (2015)
The Negishi palladium-catalyzed cross-coupling reaction between 3-ethoxy-4-iodo-1H-pyrazole and various benzylzinc halides was extensively studied. Using simplified, robust, and optimized reaction conditions, a series of electron-poor benzylzinc halides w
