5870-62-2 Usage
Uses
Used in Pharmaceutical Industry:
3-hydroxycyclopent-2-en-1-one is used as a key building block in the synthesis of various pharmaceuticals and natural products. Its unique structure and functional groups make it a valuable intermediate in the development of new drugs and therapeutic agents.
Used in Flavoring Agent Applications:
3-hydroxycyclopent-2-en-1-one is used as a flavoring agent in the food industry due to its sweet odor. Its unique aroma profile can be utilized to enhance the taste and aroma of various food products, contributing to a more enjoyable consumer experience.
Used in Organic Synthesis:
3-hydroxycyclopent-2-en-1-one is used as a versatile building block in organic synthesis for the production of a wide range of compounds. Its reactivity and functional groups make it a valuable component in the synthesis of complex organic molecules, including pharmaceuticals, agrochemicals, and specialty chemicals.
Used in Antioxidant and Anti-inflammatory Applications:
3-hydroxycyclopent-2-en-1-one has been studied for its potential pharmacological properties, including its antioxidant and anti-inflammatory effects. It can be used as a therapeutic agent or incorporated into formulations to provide health benefits, such as reducing oxidative stress and inflammation in various conditions.
Check Digit Verification of cas no
The CAS Registry Mumber 5870-62-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,8,7 and 0 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 5870-62:
(6*5)+(5*8)+(4*7)+(3*0)+(2*6)+(1*2)=112
112 % 10 = 2
So 5870-62-2 is a valid CAS Registry Number.
InChI:InChI=1/C16H15FN2O3/c1-22-15(20)9-11-19(14-4-2-3-10-18-14)16(21)12-5-7-13(17)8-6-12/h2-8,10H,9,11H2,1H3
5870-62-2Relevant academic research and scientific papers
A simple synthesis of 1,3-cyclopentanedione
Fuchs,McGarrity
, p. 373 - 374 (2007/10/02)
1,3-Cyclopentanedione was prepared by a simple procedure from methyl (E)-4-chloro-3-methoxy-2-butenoate via trimethyl (E)-3-methoxy-3-butene-1,1,4-tricarboxylate.