39510-50-4 Usage
General Description
2,2,2-trifluoro-N-(6-oxo-6-phenylhexyl)acetamide is a synthetic organic compound that contains fluorine, nitrogen, oxygen, and carbon atoms. It is a derivative of acetamide and contains a trifluoromethyl group attached to the nitrogen atom. The molecule also has a phenyl group attached to the sixth carbon of the hexyl chain. This chemical is often used as a building block in pharmaceutical research and can be utilized in the development of new drugs and therapeutic agents. Additionally, the trifluoromethyl group in this compound can impart unique physicochemical and pharmacological properties, making it valuable for medicinal chemistry applications.
Check Digit Verification of cas no
The CAS Registry Mumber 39510-50-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,9,5,1 and 0 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 39510-50:
(7*3)+(6*9)+(5*5)+(4*1)+(3*0)+(2*5)+(1*0)=114
114 % 10 = 4
So 39510-50-4 is a valid CAS Registry Number.
39510-50-4Relevant articles and documents
Chemoenzymatic Synthesis of Substituted Azepanes by Sequential Biocatalytic Reduction and Organolithium-Mediated Rearrangement
Zawodny, Wojciech,Montgomery, Sarah L.,Marshall, James R.,Finnigan, James D.,Turner, Nicholas J.,Clayden, Jonathan
supporting information, p. 17872 - 17877 (2019/01/04)
Enantioenriched 2-aryl azepanes and 2-arylbenzazepines were generated biocatalytically by asymmetric reductive amination using imine reductases or by deracemization using monoamine oxidases. The amines were converted to the corresponding N′-aryl ureas, which rearranged on treatment with base with stereospecific transfer of the aryl substituent to the 2-position of the heterocycle via a configurationally stable benzyllithium intermediate. The products are previously inaccessible enantioenriched 2,2-disubstituted azepanes and benzazepines.
