10310-60-8 Usage
General Description
1-butyl-3-ethylurea is a chemical compound that belongs to the class of urea derivatives. It is composed of a butyl group and an ethyl group attached to the nitrogen atom of the urea molecule. 1-butyl-3-ethylurea is used in various applications such as solvents, electrolytes in lithium batteries, and as a potential drug for the treatment of neurodegenerative diseases. Its unique chemical structure allows it to exhibit different properties, such as high thermal stability, low volatility, and high conductivity, making it a versatile compound in various industrial and scientific applications. Additionally, its potential use as a drug candidate makes it an important compound for pharmaceutical research and development.
Check Digit Verification of cas no
The CAS Registry Mumber 10310-60-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,3,1 and 0 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 10310-60:
(7*1)+(6*0)+(5*3)+(4*1)+(3*0)+(2*6)+(1*0)=38
38 % 10 = 8
So 10310-60-8 is a valid CAS Registry Number.
10310-60-8Relevant articles and documents
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Schultz
, p. 1057 (1947)
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Synthesis and application of a new fluorous-tagged ammonia equivalent
Nielsen, Simon D.,Smith, Garrick,Begtrup, Mikael,Kristensen, Jesper L.
supporting information; experimental part, p. 4557 - 4566 (2010/08/20)
A novel fluorous-tagged ammonia equivalent has been developed. It is based on a nitrogen-oxygen bond, which can be cleaved in a traceless manner by a molybdenum complex or samarium diiodide. The application in the synthesis of ureas, amides, sulfonamides, and carbamates is described. The scope of the fluo-rous N-O linker is exemplified by the synthesis of itopride, a drug used for the treatment of functional dyspepsia. Itopride was synthesized with the aid of fluorous purification methods and the product was isolated in good overall yield, with high purity.
Process for the N-alkylation or ureas
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, (2008/06/13)
Process for the N-alkylation of ureas by reacting a urea with an alkylating agent in the presence of a solid base and a phase transfer catalyst in a diluent.
