72250-01-2 Usage
Uses
Used in Pharmaceutical Industry:
3-Hydroxydihydro-2H-pyran-4(3H)-one is utilized as an intermediate in the synthesis of organic compounds, particularly in the development of pharmaceuticals. Its unique structure and reactivity contribute to the creation of new drug molecules, potentially leading to advancements in medical treatments.
Used in Agricultural Industry:
In agriculture, 3-Hydroxydihydro-2H-pyran-4(3H)-one serves as a key intermediate in the production of various agrochemicals. Its role in synthesizing compounds with biological activity can lead to the development of novel pesticides, herbicides, or other agricultural chemicals that improve crop protection and yield.
Used in Chemical Industry:
3-hydroxydihydro-2H-pyran-4(3H)-one is also employed within the chemical industry as a versatile building block for synthesizing a range of organic compounds. Its cyclic structure and functional groups make it suitable for use in the creation of specialty chemicals, polymers, and other materials with specific properties for various applications.
Used for Research and Development:
3-Hydroxydihydro-2H-pyran-4(3H)-one is an interesting target for research and development efforts due to its potential biological activities. Scientists are exploring its interactions with biological systems to uncover new applications in medicine, agriculture, and other fields, further expanding its utility and impact.
Check Digit Verification of cas no
The CAS Registry Mumber 72250-01-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,2,2,5 and 0 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 72250-01:
(7*7)+(6*2)+(5*2)+(4*5)+(3*0)+(2*0)+(1*1)=92
92 % 10 = 2
So 72250-01-2 is a valid CAS Registry Number.
72250-01-2Relevant academic research and scientific papers
Preparation of α-oxygenated ketones by the dioxygenation of alkenyl boronic acids
Patil, Aditi S.,Mo, Dong-Liang,Wang, Heng-Yen,Mueller, Daniel S.,Anderson, Laura L.
supporting information; experimental part, p. 7799 - 7803 (2012/09/08)
Two in two: Dioxygenation of alkenyl boronic acids has been achieved with N-hydroxyphthalimide. The two-step process involves etherification of an alkenyl boronic acid with N-hydroxyphthalimide followed by a [3,3] rearrangement. The dioxygenated product can then be hydrolyzed to form either the corresponding α-hydroxy ketone or the α-benzoyloxy ketone. Copyright
Design, synthesis, and structure-activity relationship of novel CCR2 antagonists
Kothandaraman, Shankaran,Donnely, Karla L.,Butora, Gabor,Jiao, Richard,Pasternak, Alexander,Morriello, Gregori J.,Goble, Stephen D.,Zhou, Changyou,Mills, Sander G.,MacCoss, Malcolm,Vicario, Pasquale P.,Ayala, Julia M.,DeMartino, Julie A.,Struthers, Mary,Cascieri, Margaret A.,Yang, Lihu
scheme or table, p. 1830 - 1834 (2009/11/30)
A series of novel 1-aminocyclopentyl-3-carboxyamides incorporating substituted tetrahydropyran moieties have been synthesized and subsequently evaluated for their antagonistic activity against the human CCR2 receptor. Among them analog 59 was found to posses potent antagonistic activity.
