20099-95-0 Usage
Uses
Used in Pharmaceutical Industry:
1-(4-Chloro-phenyl)-2-Morpholin-4-yl-ethanone, 98+% C12H14ClNO2, MW: 239.70 is used as a building block for the synthesis of various pharmaceutical compounds due to its unique structure and properties. It plays a crucial role in the development of new drugs, contributing to the advancement of the pharmaceutical industry.
Used in Research and Development:
In the field of research and development, 1-(4-Chloro-phenyl)-2-Morpholin-4-yl-ethanone, 98+% C12H14ClNO2, MW: 239.70 is employed as a key component in the synthesis of organic compounds. Its distinctive structure allows researchers to explore new avenues in chemical synthesis, potentially leading to the creation of novel materials and compounds with a wide range of applications.
Used in Material Science:
Check Digit Verification of cas no
The CAS Registry Mumber 20099-95-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,0,9 and 9 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 20099-95:
(7*2)+(6*0)+(5*0)+(4*9)+(3*9)+(2*9)+(1*5)=100
100 % 10 = 0
So 20099-95-0 is a valid CAS Registry Number.
20099-95-0Relevant articles and documents
Solvent-Free Synthesis of α-Amino Ketones from α-Hydroxyl Ketones via A Novel Tandem Reaction Sequence Based on Heyns Rearrangement
Li, Ling-Yu,Zeng, Qing-Le,Li, Guang-Xun,Tang, Zhuo
supporting information, p. 694 - 699 (2019/03/26)
Heyns rearrangement have been famous for carbohydrate chemists for several decades. However, this reaction was underrated as a useful method for synthetic chemists due to preparative shortcomings. Herein we developed an efficient method for the synthesis of pharmaceutically important α-amino ketones from readily available α-hydroxy ketones and secondary amines through a tandem reaction sequence based on Heyns rearrangement. The reaction smoothly proceeded by using catalytic PTSA as catalyst without solvent. Primary and secondary α-hydroxy ketones were readily used and regioselectively afforded the correspondingly α-amino ketones with moderate yield.
