73847-53-7 Usage
Uses
Used in Chemical Synthesis Industry:
Benzenamine, 3-ethenyl-, hydrochloride is used as a chemical intermediate for the production of dyes, which are essential for coloring textiles, plastics, and other materials. Its presence in the synthesis process contributes to the creation of a wide range of colorants that enhance the aesthetic and functional properties of various products.
Used in Pharmaceutical Industry:
In the pharmaceutical sector, Benzenamine, 3-ethenyl-, hydrochloride serves as a key intermediate in the synthesis of certain medications. Its involvement in drug development is crucial for the production of effective treatments and therapies that address various health conditions.
Used in Agricultural Chemicals Industry:
Benzenamine, 3-ethenyl-, hydrochloride is also utilized as an intermediate in the manufacturing of agricultural chemicals. Its role in this industry is vital for the development of products that contribute to crop protection and enhancement of agricultural yields, thereby supporting food security and sustainable farming practices.
Check Digit Verification of cas no
The CAS Registry Mumber 73847-53-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,8,4 and 7 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 73847-53:
(7*7)+(6*3)+(5*8)+(4*4)+(3*7)+(2*5)+(1*3)=157
157 % 10 = 7
So 73847-53-7 is a valid CAS Registry Number.
73847-53-7Relevant academic research and scientific papers
Highly chemo- and regioselective reduction of aromatic nitro compounds using the system silane/oxo-rhenium complexes
De Noronha, Rita G.,Romao, Carlos C.,Fernandes, Ana C.
supporting information; experimental part, p. 6960 - 6964 (2010/03/03)
(Chemical Equation Presented) The reduction of aromatic nitro compounds to the corresponding amines with silanes catalyzed by high valent oxo-rhenium complexes is reported. The catalytic systems PhMe2SiH/ReIO 2(PPh3)2 (5 mol %) and PhMe2SiH/ ReOCl3(PPh3)2 (5 mol %) reduced efficiently a series of aromatic nitro compounds in the presence of a wide range of functional groups such as ester, halo, amide, sulfone, lactone, and benzyl. This methodology also allowed the regioselective reduction of dinitrobenzenes to the corresponding nitroanilines and the reduction of an aromatic nitro group in presence of an aliphatic nitro group. 2009 American Chemical Society.
