52696-91-0 Usage
Uses
Used in Lithium-Ion Battery Industry:
1-BUTYL-3,3-DIMETHYLUREA is used as an additive to improve the performance and stability of lithium-ion batteries. Its incorporation enhances the overall efficiency and longevity of these batteries, making them more reliable for various applications.
Used in Organic Synthesis:
1-BUTYL-3,3-DIMETHYLUREA serves as a solvent in organic synthesis, facilitating chemical reactions and aiding in the production of a range of organic compounds. Its properties make it a preferred choice for chemists working in research and development.
Used in Metalworking Fluids:
As a corrosion inhibitor in metalworking fluids, 1-BUTYL-3,3-DIMETHYLUREA helps to prevent the degradation of metal surfaces during manufacturing processes. This contributes to the maintenance of tool integrity and extends the lifespan of machinery.
Used in Pharmaceutical and Medicinal Chemistry Research:
1-BUTYL-3,3-DIMETHYLUREA is utilized in research laboratories for its potential applications in the development of pharmaceuticals and medicines. Its unique properties make it a valuable compound for exploring new therapeutic agents and treatment modalities.
Check Digit Verification of cas no
The CAS Registry Mumber 52696-91-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,6,9 and 6 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 52696-91:
(7*5)+(6*2)+(5*6)+(4*9)+(3*6)+(2*9)+(1*1)=150
150 % 10 = 0
So 52696-91-0 is a valid CAS Registry Number.
InChI:InChI=1/C7H16N2O/c1-4-5-6-8-7(10)9(2)3/h4-6H2,1-3H3,(H,8,10)
52696-91-0Relevant academic research and scientific papers
N-Nitroso- and N-Nitrotrialkylureas and Their Decomposition
White, Emil H.,Ryan, Thomas J.,Hahn, Bo Sup,Erickson, Ronald H.
, p. 4860 - 4866 (2007/10/02)
The synthesis and decomposition of N-(n-butyl)-N',N'-dimethyl-N-nitrosourea (2a), N-(n-butyl)-N',N'-dimethyl-N-nitrourea (3a), N',N'-dimethyl N-(1-norbornyl)-N-nitrosourea (2b), N',N'-dimethyl-N-(1-norbornyl)-N-nitrourea (3b) are described.Several of the compounds show complex NMR spectra ascribable to rotational isomerism.Decomposition of 2a and 3a gave n-butyl N,N-dimethylcarbamate and tetramethylurea, while decompostion of 2b and 3b in methylene chloride gave 1-norbornyl N,N-dimethylcarbamate and 1-norbornyl chloride.These products are formed via diazotic acid derivatives and carbonium ion pairs; the reaction mechanism is essentially the same as that established for the closely related N-nitrosoamides.In concentrated solutions, nitrosourea 2a yielded a new product, amino acid 20.
