3314-49-6 Usage
Uses
Used in Organic Synthesis:
N-OCTYLLITHIUM is used as a reagent for the formation of carbon-carbon bonds, which is crucial in the synthesis of complex organic compounds. Its strong nucleophilic nature allows it to participate in various organic reactions, facilitating the formation of desired products in chemical research and industrial applications.
Used in Chemical Research:
In the field of chemical research, N-OCTYLLITHIUM is employed as a key component in the development and understanding of new chemical reactions and mechanisms. Its unique properties enable scientists to explore novel pathways and synthesize new compounds with potential applications in various industries.
Used in Industrial Processes:
N-OCTYLLITHIUM plays a significant role in industrial processes, particularly in the production of specialty chemicals and pharmaceuticals. Its ability to form carbon-carbon bonds is essential for the synthesis of complex molecules that are difficult to produce using traditional methods.
Safety Measures:
Given the highly reactive nature of N-OCTYLLITHIUM, it is imperative to implement rigorous safety measures during its use. This includes handling the compound under an inert atmosphere to prevent unwanted reactions with air or moisture. Additionally, proper storage and disposal protocols must be followed to minimize the risk of accidents and ensure the safety of personnel involved in its use.
Check Digit Verification of cas no
The CAS Registry Mumber 3314-49-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,3,1 and 4 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 3314-49:
(6*3)+(5*3)+(4*1)+(3*4)+(2*4)+(1*9)=66
66 % 10 = 6
So 3314-49-6 is a valid CAS Registry Number.
3314-49-6Relevant academic research and scientific papers
Alkyllithium Reagents from Alkyl Halides and Lithium Radical Anions
Freeman, Peter K.,Hutchinson, Larry L.
, p. 1924 - 1930 (2007/10/02)
The reaction of alkyl halides with three different lithium radical anions, lithium naphthalene (LiN), lithium di-tert-butylnaphthalene (LiDBN), and lithium di-tert-butylbiphenyl (LiDBB), was studied.The reaction of alkyl halides with an excess of LiN, LiDBN, or LiDBB in THF at -78 deg C leads to a consistently high yield (96-100percent) of reduction products (RH, RLi) with a high degree of formation of RLi (anion trapping 93-95percent) in the case of LiDBB.LiDBN consistently produces high yields of reduction products (89-99percent) with widely variable amounts of anion trapping (21-88percent), while LiN provides variable yields of reduction (39-99percent) and anion trapping (24-65percent).Variation of the concentration of lithium bromide and naphthalene and the ratio of alkyl halide to naphthalene in conjunction with the use of deuterium tracer experiments provided evidence consistent with a competition between metalation of the lithium dihydronaphthalenedicarboxylate by alkyllithium and carbonation of alkyllithium in the carbonation step of the analysis.
