30289-16-8 Usage
Uses
Used in Organic Synthesis:
(diethylamino)([(1Z)-1-phenylethylidene]aminooxy)methanone is used as a synthetic intermediate for the creation of various complex organic molecules. Its unique structure and functional groups make it a valuable building block in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, (diethylamino)([(1Z)-1-phenylethylidene]aminooxy)methanone is used as a key component in the development of novel drugs. Its structural diversity and the presence of multiple functional groups allow for the design of innovative therapeutic agents with potential applications in treating various diseases and medical conditions.
Used in Material Science:
(diethylamino)([(1Z)-1-phenylethylidene]aminooxy)methanone may also find applications in the field of material science, where its unique structure and properties can be utilized to develop new materials with specific characteristics, such as improved mechanical strength, thermal stability, or chemical resistance.
Check Digit Verification of cas no
The CAS Registry Mumber 30289-16-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,0,2,8 and 9 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 30289-16:
(7*3)+(6*0)+(5*2)+(4*8)+(3*9)+(2*1)+(1*6)=98
98 % 10 = 8
So 30289-16-8 is a valid CAS Registry Number.
30289-16-8Relevant academic research and scientific papers
Dissociation or cyclization: Options for a triad of radicals released from oxime carbamates
McBurney, Roy T.,Walton, John C.
supporting information, p. 7349 - 7354 (2013/06/27)
A set of oxime carbamates having N-alkyl and N,N-dialkyl substituents were prepared via carbonyldiimidazole intermediates. It was shown by EPR spectroscopy that they underwent clean homolysis of their N-O bonds upon UV photolysis. During photolysis of acetophenone O-allylcarbamoyl oxime, the corresponding oxazolidin-2-onylmethyl radical was detected by EPR spectroscopy, providing the first evidence that N-monosubstituted carbamoyloxyl radicals can hold their structural integrity. N,N-Disubstituted carbamoyloxyl radicals dissociated rapidly at the lowest accessible temperatures. Above room temperature, both types of oxime carbamate acted as selective new precursors for aminyl and iminyl radicals. Rate parameters were measured for 5-exo cyclization of N-benzyl-N-pent-4-enylaminyl radicals; the rate constant was smaller than for C-centered and O-centered analogues. Oxime carbamates derived from the volatile diethylamine afforded aryliminyl radicals that proved convenient for phenanthridine preparations.
