672-74-2 Usage
Uses
Used in Pharmaceutical Industry:
Ethenyl 3-nitrobenzoate is utilized as an intermediate in the synthesis of various pharmaceuticals, contributing to the development of new medications due to its ability to participate in a range of chemical reactions that facilitate the creation of diverse drug molecules.
Used in Agrochemical Industry:
In the agrochemical sector, ethenyl 3-nitrobenzoate is employed as a precursor in the production of agrochemicals, playing a crucial role in the synthesis of compounds that are vital for crop protection and enhancement of agricultural yields.
Used in Dye Industry:
Ethenyl 3-nitrobenzoate is harnessed as a key component in the formulation of dyes, where its chemical properties allow for the creation of a spectrum of colors used in various applications, including textiles and other industrial processes.
Used in Organic Synthesis:
As a building block in organic synthesis, ethenyl 3-nitrobenzoate is used as a reactant for the preparation of a wide array of organic compounds, showcasing its versatility and importance in the synthesis of complex molecules for multiple applications across different industries.
Check Digit Verification of cas no
The CAS Registry Mumber 672-74-2 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,7 and 2 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 672-74:
(5*6)+(4*7)+(3*2)+(2*7)+(1*4)=82
82 % 10 = 2
So 672-74-2 is a valid CAS Registry Number.
672-74-2Relevant academic research and scientific papers
Ethenolate transfer reactions: A facile synthesis of vinyl esters
Appaye, Srinivasan Kaliyaperumal,Nikumbh, Satish Pandurang,Govindapur, Rajeshwar Reddy,Banerjee, Shyamapada,Bhalerao, Dinesh S.,Kumar, Unniaran K. Syam
, p. 1115 - 1122 (2014/09/17)
A simple and efficient metal-free ethenolate transfer reaction has been elaborated in moderate-to-high yields from vinyl acetate. This reaction was accomplished by generation of potassium ethenolate, which was then reacted with homo and mixed anhydrides of aliphatic, aryl and heteroaryl acids, to yield the corresponding vinyl esters. The utility of thus generated vinyl esters was then probed by carrying out intramolecular Heck reactions to give isobenzofuran-1(3H)-one derivatives in excellent yields. Copyright
Copper(II)-catalyzed esterification of arenecarboxylic acids with aryl- and vinyl-substituted trimethoxysilanes
Luo, Fang,Pan, Changduo,Qian, Pengcheng,Cheng, Jiang
supporting information; experimental part, p. 2005 - 2010 (2010/08/19)
In this paper, the copper(II)-catalyzed esterification reaction of arenecarboxylic acids with aryl- or vinyl-substituted trimethoxysilanes is described. A series of aryltrimethoxysilanes and arenecarboxylic acids worked well under this procedure, affording aryl benzoate derivatives in moderate to good yields. Notably, trimethoxy(vinyl)silanes also worked well under this procedure giving a facile and versatile method to access vinyl benzoate derivatives. Georg Thieme Verlag Stuttgart.
