33931-42-9 Usage
Uses
Used in Nuclear Fuel Reprocessing:
N,N,N',N'-TETRAETHYLMALONAMIDE is used as a reagent in the nuclear fuel reprocessing industry for its ability to facilitate the separation and purification of nuclear materials. Its chemical properties make it suitable for handling and processing radioactive substances, contributing to the efficiency and safety of nuclear fuel reprocessing operations.
Used in Chemistry Applications:
In the field of chemistry, N,N,N',N'-TETRAETHYLMALONAMIDE serves as a versatile compound for various applications. Its unique structure and properties allow it to be used in the synthesis of other organic compounds, as well as in analytical chemistry for the detection and quantification of specific substances. Its solubility in water and stability under ordinary conditions make it a valuable asset in a wide range of chemical processes and reactions.
Check Digit Verification of cas no
The CAS Registry Mumber 33931-42-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,3,9,3 and 1 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 33931-42:
(7*3)+(6*3)+(5*9)+(4*3)+(3*1)+(2*4)+(1*2)=109
109 % 10 = 9
So 33931-42-9 is a valid CAS Registry Number.
33931-42-9Relevant academic research and scientific papers
Cobalt-catalyzed aminocarbonylation of geminal dihaloalkanes. Formation of 2-aminoamide and malonamide derivatives
Miyashita,Kawashima,Kaji,Nomura,Nohira
, p. 781 - 784 (2007/10/02)
Co2(CO)8 catalyzed aminocarbonylation of geminal dihaloalkanes R2CX2 (R = H, CH3; X = Br, Cl) with NHEt2 affording R2C(NEt2)CONEt2 selectively in n-C6H14 using NEt3, while the yield of R2C(CONEt2)2 fairly increased in THF or benzene in aid of K2CO3.
2H-1,4-BENZOTIAZINE 3-(DIALCHILAMMINO)SOSTITUITE
Balbi, A.,Ferreccio, R.,Braccio, M. Di,Mazzei, M.,Roma, G.
, p. 955 - 962 (2007/10/02)
Reaction of 2-aminothiophenol with N,N,N',N'-tetrasubstituted 2-bromomalonamides (I), in the presence of sodium hydroxide, gave 2-malonamides (II) which in turn were converted into N,N-dialkyl-3-(dialkylamino)-2H-benzothiazine-2-carbo
