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1-Propyn-1-aminium, N,N,N-triethyl-3-methoxy-3-oxo-, bromide is a complex organic compound with the chemical formula C10H18BrNO2. It is a derivative of 1-propyn-1-aminium, featuring a triethylamine group attached to the nitrogen atom, a methoxy group at the 3-position, and a carbonyl group at the 3-position as well. The compound is characterized by its bromide counterion, which contributes to its overall charge and solubility properties. This chemical is primarily used in the synthesis of various organic compounds and pharmaceuticals, owing to its unique structure and reactivity. It is important to handle 1-Propyn-1-aminium, N,N,N-triethyl-3-methoxy-3-oxo-, bromide with care, as it may have potential health and environmental impacts due to its chemical nature.

95081-59-7

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95081-59-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 95081-59-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,5,0,8 and 1 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 95081-59:
(7*9)+(6*5)+(5*0)+(4*8)+(3*1)+(2*5)+(1*9)=147
147 % 10 = 7
So 95081-59-7 is a valid CAS Registry Number.

95081-59-7Downstream Products

95081-59-7Relevant academic research and scientific papers

YNAZIRIDINES. METHODS OF SYNTHESIS OF A NEW TYPE OF YNAMINES

Tikhomirov, D. A.,Shubina, Yu. V.,Eremeev, A. V.

, p. 1231 - 1235 (1984)

Ways of synthesizing ynaziridines by succesive halogenation and dehydrohalogenation of enaziridino esters, the reaction of potassium aziridinide with bromophenylacetylene, the reaction of 1H-aziridines with the methyl ester of bromopropionic acid was studied.The different direction of the reaction of aziridines with bromomethylpropiolate as a function of the nature of the solvent was demonstrated.In methanol the addition of aziridine to the triple bond proceeds stereospecifically with the formation of the E-isomer.When this reaction was conducted in ether, ynaziridines were obtained for the first time.An effective method of synthesis of ynaminoesters was developed.

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