1221341-52-1 Usage
Description
3-Cyclopentyl-N-methoxy-N-methylpropanamide, also known as Pregabalin, is a chemical compound belonging to the amide class of organic compounds. It has a molecular formula of C10H19NO2 and is used as a medication for various neurological conditions.
Used in Pharmaceutical Industry:
3-Cyclopentyl-N-methoxy-N-methylpropanamide is used as an anticonvulsant and analgesic medication for the treatment of epilepsy, neuropathic pain, fibromyalgia, and generalized anxiety disorder. It works by blocking certain neurotransmitters in the brain that are involved in pain signals and reducing the abnormal electrical activity in the brain that can cause seizures, thus providing relief from nerve pain and anti-anxiety effects.
Used in Neurological Treatment:
3-Cyclopentyl-N-methoxy-N-methylpropanamide is used as a therapeutic agent for managing neurological conditions by modulating the transmission of pain signals and reducing seizure activity in the brain. This makes it a valuable medication for patients suffering from chronic pain and anxiety disorders.
Check Digit Verification of cas no
The CAS Registry Mumber 1221341-52-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,2,1,3,4 and 1 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1221341-52:
(9*1)+(8*2)+(7*2)+(6*1)+(5*3)+(4*4)+(3*1)+(2*5)+(1*2)=91
91 % 10 = 1
So 1221341-52-1 is a valid CAS Registry Number.
1221341-52-1Relevant articles and documents
Site-Selective Pd-Catalyzed C(sp3)?H Arylation of Heteroaromatic Ketones
Kudashev, Anton,Baudoin, Olivier
supporting information, p. 17688 - 17694 (2021/11/16)
A ligand-controlled site-selective C(sp3)?H arylation of heteroaromatic ketones has been developed using Pd catalysis. The reaction occurred selectively at the α- or β-position of the ketone side-chain. The switch from α- to β-arylation was realized by addition of a pyridone ligand. The α-arylation process showed broad scope and high site- and chemoselectivity, whereas the β-arylation was more limited. Mechanistic investigations suggested that α-arylation occurs through C?H activation/oxidative addition/reductive elimination whereas β-arylation involves desaturation and aryl insertion.
