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O-nitrosobistrifluormethylhydroxylamin, also known as bis(trifluoromethyl)nitrosamine or CF3N(O)NO, is a highly reactive and potentially hazardous chemical compound. It is an oily, colorless liquid with a pungent odor and is formed by the reaction of bis(trifluoromethyl)hydroxylamine with nitrous acid. O-nitrosobistrifluormethylhydroxylamin is known for its instability and can decompose explosively upon heating or upon contact with certain substances. Due to its reactivity, it is not used commercially and is primarily of interest in chemical research. It is important to handle O-nitrosobistrifluormethylhydroxylamin with extreme caution, as it can pose significant health and safety risks.

359-75-1

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359-75-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 359-75-1 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,5 and 9 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 359-75:
(5*3)+(4*5)+(3*9)+(2*7)+(1*5)=81
81 % 10 = 1
So 359-75-1 is a valid CAS Registry Number.

359-75-1Relevant academic research and scientific papers

Nitroxide Chemistry. Part 13. Reaction of NN-Bis(trifluoromethyl)amino-oxyl with Hexafluoroisopropylideneimine and Related Compounds

Fisher, Raymond,Haszeldine, Robert N.,Tipping, Anthony E.

, p. 406 - 409 (2007/10/02)

The initial product from reaction of the oxyl (CF3)2N-O. with hexafluoroisopropylideneimine is the substituted imine (CF3)2C=N-O-N(CF3)2 (isolated in 81percent yield) which, via further oxyl attack at carbon, gives the compounds (CF3)2CO, (CF3)2N-NO, (CF3)2N-O-N(CF3)2, and (CF3)2N-O-C(CF3)2N+(O-)=N-C(CF3)2-O-N(CF3)2.Oxyl attack on hexafluoroacetone oxime affords as major products (CF3)2CO, (CF3)2NH, and (CF3)2N-O-NO.The oxyl reacts with hexafluoroacetone anil to yield a hexaoxyl adduct, with hexafluoroacetone hydrazone to afford the diazoalkane (CF3)2CN2 (100percent), and with hexafluoroacetone azine to give the bis-1:4-adduct (CF3)2N-O-C(CF3)2-N=N-C(CF3)2-O-N(CF3)2 (100percent).Thus, initial radical attack of the oxyl invariably takes place at carbon in the series of imines studied.

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