1119450-19-9 Usage
Uses
Used in Organic Synthesis:
1-(2-bromobutanoyl)pyrrolidine is utilized as a key intermediate in the synthesis of various organic compounds. Its unique structure allows for the creation of a diverse range of molecules, making it a valuable asset in the field of organic chemistry.
Used in Medicinal Chemistry Research:
In the realm of medicinal chemistry, 1-(2-bromobutanoyl)pyrrolidine serves as a crucial building block for the development of novel pharmaceutical drugs. Its potential application in drug discovery has attracted the attention of researchers, who are investigating its properties and interactions with biological targets.
Used in Pharmaceutical Drug Development:
1-(2-bromobutanoyl)pyrrolidine holds promise for the development of new pharmaceutical drugs due to its unique structure and properties. Researchers are actively exploring its potential in creating innovative therapeutic agents that can address various medical conditions.
Used in Chemical Research and Development:
1-(2-bromobutanoyl)pyrrolidine is also employed in chemical research and development, where it is used to study its reactivity, stability, and potential applications in creating new materials and compounds.
Check Digit Verification of cas no
The CAS Registry Mumber 1119450-19-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,1,9,4,5 and 0 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1119450-19:
(9*1)+(8*1)+(7*1)+(6*9)+(5*4)+(4*5)+(3*0)+(2*1)+(1*9)=129
129 % 10 = 9
So 1119450-19-9 is a valid CAS Registry Number.
1119450-19-9Relevant articles and documents
Transition-Metal-Free Coupling of Alkynes with α-Bromo Carbonyl Compounds: An Efficient Approach towards β,γ-Alkynoates and Allenoates
Liu, Wenbo,Chen, Zhengwang,Li, Lu,Wang, Haining,Li, Chao-Jun
supporting information, p. 5888 - 5893 (2016/04/26)
A direct transition-metal-free coupling between alkynes and α-bromo carbonyl compounds has been developed with ultraviolet (UV) light in aqueous media. This method represents a facile approach to synthetically useful β,γ-alkynyl esters and amides stereoselectively from two readily available starting materials. As an example of the synthetic application of the products, the alkynyl esters were readily converted into allenoates. Time for UV! A direct coupling between alkynes and α-bromo compounds has been developed with ultraviolet light in aqueous media (see scheme). This method represents a facile approach to synthetically useful β,γ-alkynyl esters and amides stereoselectively from two readily available starting materials.
