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166192-72-9

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166192-72-9 Usage

Structure

Bicyclic organic compound with a nitrogen heterocycle

Nitrogen heterocycle

Contains three nitrogen atoms in the ring

Nitro group

Presence of a nitro (-NO2) functional group

Ethyl group

Contains an ethyl (-CH2CH3) group attached to the bicyclic structure

Potential applications

Organic synthesis and pharmaceutical research

Building block

Can be used as a building block for the synthesis of other organic molecules

Reagent

May be used as a reagent in chemical reactions

Specific properties

Depends on the specific context and application within the field of organic chemistry

Check Digit Verification of cas no

The CAS Registry Mumber 166192-72-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,6,1,9 and 2 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 166192-72:
(8*1)+(7*6)+(6*6)+(5*1)+(4*9)+(3*2)+(2*7)+(1*2)=149
149 % 10 = 9
So 166192-72-9 is a valid CAS Registry Number.

166192-72-9Downstream Products

166192-72-9Relevant articles and documents

Synthesis and transformations of 1,3,5-triazabicyclohexanes

Makhova,, N. N.,Mikhailyuk, A. N.,Bova, A. E.,Chabina, T. V.,Khmel'nitskii, L. I.

, p. 2004 - 2009 (1993)

The conditions for the condensation of 1,2-nonsubstituted diaziridines with CH2O and NH3 (or AlkNH2) to the corresponding 1,3,5-triazabicyclohexanes have been found and 3-phenylsulfonyl, 3-trimethylsilyl, 3-nitroso, and 3-nitro derivatives of the latter have been obtained. - Key words: diaziridines, condensation; 1,3,5-triazabicyclohexanes, α-aminomethylation, nitrosation, denitrosation, silylation, nitration.

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