13067-81-7 Usage
Uses
Used in Organic Synthesis:
2-Ethylhexyllithium is used as a strong base and nucleophile for the formation of carbon-carbon bonds and the synthesis of complex organic molecules. Its reactivity allows for the creation of new chemical structures that are otherwise difficult to achieve.
Used in Chemical Research:
In the field of chemical research, 2-Ethylhexyllithium is employed as a reagent to study the properties and reactions of organometallic compounds. Its unique characteristics provide insights into the behavior of lithiated alkyl compounds and their interactions with other chemical entities.
Used in Pharmaceutical Industry:
2-Ethylhexyllithium is used as a key intermediate in the synthesis of certain pharmaceutical compounds. Its ability to form carbon-carbon bonds and act as a nucleophile is crucial in the development of new drugs and medicinal agents.
Used in Material Science:
In material science, 2-Ethylhexyllithium is utilized in the synthesis of advanced materials with specific properties. Its reactivity and nucleophilic nature contribute to the creation of novel materials with potential applications in various industries.
Used in Specialty Chemicals Production:
2-Ethylhexyllithium is used as a reactant in the production of specialty chemicals, where its reactivity and nucleophilic properties are harnessed to create unique chemical entities for specific applications.
Check Digit Verification of cas no
The CAS Registry Mumber 13067-81-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,0,6 and 7 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 13067-81:
(7*1)+(6*3)+(5*0)+(4*6)+(3*7)+(2*8)+(1*1)=87
87 % 10 = 7
So 13067-81-7 is a valid CAS Registry Number.
13067-81-7Relevant articles and documents
NMR spectra of a hydrocarbon-soluble organosodium compound and its lithium analogs
Pakuro,Arest-Yakubovich,Shcheglova,Petrovsky,Chekulaeva
, p. 838 - 840 (1996)
1H, 23Na, and 7Li NMR spectra of 2-ethylhexylsodium, 2-ethylhexyllithium, and isobutyllithium obtained in the reaction of the corresponding alkyl chlorides and metals have been recorded. The 1H NMR signal for the protons of the CH2Na group is shifted upfield compared with that for the protons of the CH2Li group (doublets at δ -0.88 and δ -0.83, respectively). The composition of the products of reaction of 2-ethylhexyl chloride with sodium depends on the form of the metal reagent employed. The use of sodium balls with diameter up to 2 mm results in the formation of products containing ionic chlorine (30-50 % with respect to Na); the reaction with the dispersion proceeds faster and the reaction product is chlorine-free. The 23Na NMR spectra of these substances are also different, which is explained by the formation of 2-ethylhexylsodium complexes with NaCl in the former case.
