1214375-69-5 Usage
Uses
Used in Organic Synthesis:
Ethyl 2,6-dibromobenzoate is utilized as a reagent in organic synthesis for the production of various chemical compounds. Its unique structure allows it to be a valuable intermediate in the synthesis of pharmaceuticals, fragrances, and other specialty chemicals.
Used in the Food Industry:
In the food industry, Ethyl 2,6-dibromobenzoate is employed as a flavoring agent to impart specific tastes and aromas to food products. Its use in this application is due to its ability to enhance the sensory characteristics of various food items.
Used in Pharmaceutical Production:
Ethyl 2,6-dibromobenzoate is also used in the production of pharmaceuticals. Its role in this industry is to serve as a building block for the synthesis of various drug molecules, contributing to the development of new medications and therapies.
Used in Fragrance Industry:
In the fragrance industry, Ethyl 2,6-dibromobenzoate is used to create unique and complex scents. Its chemical properties allow it to be incorporated into perfumes, colognes, and other scented products, adding depth and complexity to the final fragrance.
Check Digit Verification of cas no
The CAS Registry Mumber 1214375-69-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,1,4,3,7 and 5 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1214375-69:
(9*1)+(8*2)+(7*1)+(6*4)+(5*3)+(4*7)+(3*5)+(2*6)+(1*9)=135
135 % 10 = 5
So 1214375-69-5 is a valid CAS Registry Number.
1214375-69-5Relevant academic research and scientific papers
Noncovalent Interactions in Ir-Catalyzed C-H Activation: L-Shaped Ligand for Para-Selective Borylation of Aromatic Esters
Hoque, Md Emdadul,Bisht, Ranjana,Haldar, Chabush,Chattopadhyay, Buddhadeb
supporting information, p. 7745 - 7748 (2017/06/21)
An efficient strategy for the para-selective borylation of aromatic esters is described. For achieving high para-selectivity, a new catalytic system has been developed modifying the core structure of the bipyridine. It has been proposed that the L-shaped ligand is essential to recognize the functionality of the oxygen atom of the ester carbonyl group via noncovalent interaction, which provides an unprecedented controlling factor for para-selective C-H activation/borylation.
Regio- and chemoselective C-H chlorination/bromination of electron-deficient arenes by weak coordination and study of relative directing-group abilities
Sun, Xiuyun,Shan, Gang,Sun, Yonghui,Rao, Yu
supporting information, p. 4440 - 4444 (2013/05/22)
It's all relative: A practical and efficient PdII-catalyzed regio- and chemoselective chlorination/bromination has been developed for the facile synthesis of a broad range of aromatic chlorides. The reaction demonstrates excellent reactivity, good functional-group tolerance, and high yields. A preliminary study was conducted to evaluate relative directing-group abilities of various functionalities. Copyright
