499190-80-6 Usage
Derivative of imidazole
Imidazole is a five-membered heterocyclic ring containing three carbon atoms and two nitrogen atoms 1H-Imidazole,1-ethenyl-4-nitrois a modified version of this imidazole structure, with additional functional groups attached to it.
Nitro group attachment
4th carbon atom The compound features a nitro group (-NO2) attached to the 4th carbon atom of the imidazole ring, which influences its chemical reactivity and properties.
Ethenyl group attachment
1st carbon atom An ethenyl group (-CH=CH2) is attached to the 1st carbon atom of the imidazole ring, further modifying its chemical properties and reactivity.
Applications
Pharmaceutical, agrochemical, and synthesis of other organic compounds 1H-Imidazole,1-ethenyl-4-nitrois used in various fields, including the development of new drugs, agrochemicals, and as a building block for creating other organic compounds.
Properties and reactivity
Useful in the development of new materials and drugs The unique properties and reactivity of 1H-Imidazole,1-ethenyl-4-nitromake it a valuable compound for creating new materials and pharmaceuticals.
Check Digit Verification of cas no
The CAS Registry Mumber 499190-80-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,9,9,1,9 and 0 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 499190-80:
(8*4)+(7*9)+(6*9)+(5*1)+(4*9)+(3*0)+(2*8)+(1*0)=206
206 % 10 = 6
So 499190-80-6 is a valid CAS Registry Number.
499190-80-6Relevant articles and documents
Routes to N-vinyl-nitroimidazoles and N-vinyl-deazapurines
Clayton, Russell,Ramsden, Christopher A.
, p. 701 - 705 (2004)
The preparations of 4- and 5-nitro-1-vinylimidazole (2 and 7) are described. Selective reduction of the nitro group using Fe/dil HCl is achieved for the 4-nitro derivative but this is not effective when ethoxymethylenemalononitrile is used to trap the amine. For 5-nitroimidazole studies the N-vinyl substituent is kept masked as a 2-chloroethyl group, which remains unchanged during catalytic reduction of the nitro function (Pd/C), and is revealed by HCl elimination at a later stage. In this way, the 1-deazapurine 13 and the tricyclic derivative 14 have been prepared.
