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4-(Bromomethyl)-2-pyrrolidinone is an organic compound that serves as an enamine building block in the synthesis of various chemical compounds. It is characterized by its unique structure, which includes a bromomethyl group attached to a pyrrolidinone ring. This feature makes it a valuable intermediate in the production of pharmaceuticals and other specialty chemicals.

945671-51-2

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945671-51-2 Usage

Uses

Used in Pharmaceutical Industry:
4-(Bromomethyl)-2-pyrrolidinone is used as a key intermediate in the synthesis of pharmaceutical compounds, such as 6,6''-Dihydroxypregabalin Lactam (D454645), an impurity of rac-Pregabalin (P704800). Its enamine building block property allows for the creation of complex molecular structures, which are essential in the development of new drugs and therapeutic agents.
Used in Chemical Synthesis:
In the field of chemical synthesis, 4-(Bromomethyl)-2-pyrrolidinone is utilized as a versatile building block for the production of a wide range of specialty chemicals. Its reactivity and functional group compatibility make it suitable for various synthetic routes, leading to the formation of diverse chemical entities with potential applications in various industries.

Check Digit Verification of cas no

The CAS Registry Mumber 945671-51-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,4,5,6,7 and 1 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 945671-51:
(8*9)+(7*4)+(6*5)+(5*6)+(4*7)+(3*1)+(2*5)+(1*1)=202
202 % 10 = 2
So 945671-51-2 is a valid CAS Registry Number.

945671-51-2Downstream Products

945671-51-2Relevant academic research and scientific papers

Discovery of orally available integrin α5β1 antagonists

Zischinsky, Gunther,Osterkamp, Frank,Vossmeyer, Doerte,Zahn, Grit,Scharn, Dirk,Zwintscher, Ariane,Stragies, Roland

scheme or table, p. 380 - 382 (2010/04/02)

Previous research within our laboratories identified the 3-hydroxypyrrolidine scaffold 1 as a new and selective integrin α5β1 inhibitor class which was designed for local administration. Herein the discovery of new orally available integrin α5β1 inhibitor scaffolds for potential systemic treatment is described.

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