850348-56-0 Usage
Uses
Used in Pharmaceutical Industry:
1-(2-BROMO-PHENYL)-2,5-DIHYDRO-1H-PYRROLE is used as a key intermediate in the synthesis of various pharmaceutical compounds. Its presence of a bromine atom allows for a range of reactions and transformations, making it a valuable component in the development of new drugs and therapeutic agents.
Used in Agrochemical Industry:
In the agrochemical industry, 1-(2-BROMO-PHENYL)-2,5-DIHYDRO-1H-PYRROLE serves as a crucial building block for the creation of various agrochemical products. Its unique structure and reactivity enable the synthesis of compounds with specific properties, such as pest control agents and plant growth regulators.
Used in Fine Chemicals Industry:
1-(2-BROMO-PHENYL)-2,5-DIHYDRO-1H-PYRROLE is also utilized in the fine chemicals industry for the production of specialty chemicals. Its versatility in organic synthesis allows for the creation of a wide range of compounds with specific applications, such as dyes, fragrances, and other high-value products.
Overall, 1-(2-BROMO-PHENYL)-2,5-DIHYDRO-1H-PYRROLE is a versatile and valuable compound in the fields of pharmaceuticals, agrochemicals, and fine chemicals, thanks to its unique structure, reactivity, and wide range of applications.
Check Digit Verification of cas no
The CAS Registry Mumber 850348-56-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,5,0,3,4 and 8 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 850348-56:
(8*8)+(7*5)+(6*0)+(5*3)+(4*4)+(3*8)+(2*5)+(1*6)=170
170 % 10 = 0
So 850348-56-0 is a valid CAS Registry Number.
850348-56-0Relevant academic research and scientific papers
Du, Hong-Jin,Lin, Chao,Wen, Xiaoan,Xu, Qing-Long
, p. 7480 - 7484 (2018)
An efficient approach to chiral α-hydroxy acid esters by Lewis acid-mediated asymmetric [1,5]-hydride shift and isomerization of 2-(3-pyrroline-1-yl)arylketone acid ester has been achieved in up to 96% yield and 94% ee. This protocol would be applied in the synthesis of chiral α-hydroxy acid derivatives with simplicity and high enantioselectivity.
