5344-89-8 Usage
Uses
Used in Organic Synthesis:
1-(2,3-dimethylbutan-2-yl)urea is used as a reactant in organic synthesis for the production of various chemical compounds. Its unique structure allows it to participate in a range of reactions, facilitating the creation of diverse products.
Used in Pharmaceuticals:
In the pharmaceutical industry, 1-(2,3-dimethylbutan-2-yl)urea is utilized as a building block for the development of new drugs. Its chemical properties make it a valuable component in the synthesis of medicinal compounds.
Used in Agricultural Chemicals:
1-(2,3-dimethylbutan-2-yl)urea is employed in the manufacturing of agricultural chemicals, where it contributes to the formulation of products designed to enhance crop protection and yield.
Used as a Stabilizer in Plastics and Rubber:
1-(2,3-dimethylbutan-2-yl)urea serves as a stabilizer in the production of plastics and rubber, improving the durability and performance of these materials.
Used as a Corrosion Inhibitor in Lubricants:
1-(2,3-dimethylbutan-2-yl)urea is used as a corrosion inhibitor in lubricants, helping to protect machinery and equipment from wear and tear.
Used as a Reagent in Chemical Reactions:
In the realm of chemical research and development, 1-(2,3-dimethylbutan-2-yl)urea is used as a reagent to facilitate specific chemical reactions, aiding in the advancement of scientific knowledge and innovation.
Check Digit Verification of cas no
The CAS Registry Mumber 5344-89-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,3,4 and 4 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 5344-89:
(6*5)+(5*3)+(4*4)+(3*4)+(2*8)+(1*9)=98
98 % 10 = 8
So 5344-89-8 is a valid CAS Registry Number.
5344-89-8Relevant academic research and scientific papers
Metal-free conversion of methane and cycloalkanes to amines and amides by employing a borylnitrene
Bettinger, Holger F.,Filthaus, Matthias,Bornemann, Holger,Oppel, Iris M.
supporting information; body text, p. 4744 - 4747 (2009/02/06)
(Chemical Equation Presented) C-H insertion: Borylnitrenes, which are generated in situ by photoylsis of azides, convert unactivated alkanes by intermolecular C-H insertion into aminoboranes (see scheme), which in turn can be reacted further to give amines or amides. The boryl group serves two purposes: it converts the nitrene into a highly reactive BN vinylidene analogue, and it is easily cleaved from the product.
AMINE DERIVATIVE WITH POTASSIUM CHANNEL REGULATORY FUNCTION, ITS PREPARATION AND USE
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Page 20-21, (2008/06/13)
The present invention provides amine derivatives represented by formula I, its isomers, racemes or optical isomers, pharmaceutical salts thereof, its amides or esters, pharmaceutical compositions containing said compounds and the preparation methods there
Synthesis of 2H- and 3H-labelled iptakalim hydrochloride
Zhang, Cheng,Yang, Rifang,Chen, Lanfu,Zhong, Bohua,Yun, Liuhong,Wang, Hai
, p. 583 - 590 (2007/10/03)
Iptakalim hydrochloride (N-(1-methylethyl)-1,1,2-trimethyl-propylamine hydrochloride) is a promising antihypertensive drug discovered and developed by Beijing Institute of Pharmacology and Toxicology. Deuterium- and tritium-labelled compounds were designed and synthesized for pharmacokinetic and pharmacological mechanism studies. A derivatization method has been employed in the synthesis procedure. Copyright
