604800-01-3 Usage
Uses
Used in Pharmaceutical Research:
(E)-1-(2-(Furan-2-yl)vinyl)cyclopropanamine is used as a chemical compound in pharmaceutical research for its potential biological activity. (E)-1-(2-(FURAN-2-YL)VINYL)CYCLOPROPANAMINE's unique structure may contribute to the development of new drugs, targeting various medical conditions.
Used in Organic Synthesis:
In the field of organic chemistry, (E)-1-(2-(Furan-2-yl)vinyl)cyclopropanamine is used as a building block for the synthesis of other organic compounds. Its cyclopropanamine derivative nature allows for its incorporation into more complex molecular structures, potentially leading to the creation of novel chemical entities with diverse applications.
Used in Drug Development:
(E)-1-(2-(Furan-2-yl)vinyl)cyclopropanamine holds potential in the development of new drugs due to its cyclopropanamine derivative structure. It may be utilized in the design and synthesis of pharmaceuticals targeting a range of therapeutic areas, pending further research into its specific biological activities and properties.
Used in Chemical Industry:
Within the chemical industry, (E)-1-(2-(Furan-2-yl)vinyl)cyclopropanamine may find applications in the production of various chemical products. Its unique structure could be leveraged to create new materials or intermediates for use in a wide array of industrial processes.
Check Digit Verification of cas no
The CAS Registry Mumber 604800-01-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,0,4,8,0 and 0 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 604800-01:
(8*6)+(7*0)+(6*4)+(5*8)+(4*0)+(3*0)+(2*0)+(1*1)=113
113 % 10 = 3
So 604800-01-3 is a valid CAS Registry Number.
604800-01-3Relevant academic research and scientific papers
Bertus, Philippe,Szymoniak, Jan
, p. 7133 - 7136 (2003)
The reaction of various aromatic nitriles with 1.1 equiv of Ti(Oi-Pr)4 and 2.2 equiv of EtMgBr followed by addition of a Lewis acid gave 1-aryl cyclopropylamines in 43-76% yields. Under similar conditions, conjugated alkene-nitriles afford 1-alkenylcyclopropylamines (42-65%).
