4513-07-9 Usage
Amide derivative
phenylacetamide group and sulfanylidene substituent
The compound is an amide derivative, which means it contains a carbonyl group (C=O) bonded to a nitrogen atom (N). In this case, the compound has a phenylacetamide group, which consists of a phenyl ring attached to an acetamide group, and a sulfanylidene substituent.
Sulfanylidene group
two methyl substituents and an oxygen atom
The sulfanylidene group in the compound contains two methyl (CH3) substituents and an oxygen atom. This group is bonded to the carbonyl carbon of the amide derivative, giving the compound its unique properties.
Potential pharmacological or biological activities
molecular structure
Due to its molecular structure, 2-(dimethyl(oxo)-λ6-sulfanylidene)-N-phenylacetamide may have potential pharmacological or biological activities. This means that the compound could interact with biological systems and have an effect on living organisms.
Applications in pharmaceutical research and drug development
further studies and investigations
The compound could be used in pharmaceutical research or drug development due to its potential pharmacological or biological activities. However, further studies and investigations may be needed to fully understand the properties and potential applications of this chemical compound.
Check Digit Verification of cas no
The CAS Registry Mumber 4513-07-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,5,1 and 3 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 4513-07:
(6*4)+(5*5)+(4*1)+(3*3)+(2*0)+(1*7)=69
69 % 10 = 9
So 4513-07-9 is a valid CAS Registry Number.
4513-07-9Relevant academic research and scientific papers
Talero, Alexánder Garay,Martins, Bruna Sim?es,Burtoloso, Antonio C. B.
, p. 7206 - 7211 (2018)
A general, mild, and versatile synthesis of the challenging α-aryl-β-ketosulfoxonium ylides has been developed for the first time, substituting traditional methods starting from diazo compounds. The arylation of easily accessible β-ketosulfoxonium ylides using aryne chemistry allowed the preparation of a large scope of the pro-chiral ylides in very good yields (40 examples; up to 85%). As applications, these ylides were smoothly converted into α-aryl ketones after desulfurization in good yields (up to 98%) as well as in other important derivatives.
