4204-99-3 Usage
Derivative of imidazole
A five-membered aromatic ring with two nitrogen atoms This describes the core structure of the compound, which is based on the imidazole ring, an important structural motif in many biologically active molecules.
Presence of functional groups
a. Nitro group (-NO2) A nitro group is attached to the imidazole ring, which can influence the compound's chemical reactivity and biological activity.
b. Fluorophenyl group (C6H4F) A phenyl ring with a fluorine atom attached, which can affect the compound's lipophilicity and electronic properties.
c. Methyl group (-CH3) A small alkyl group attached to the imidazole ring, which can influence the compound's steric properties and solubility.
Check Digit Verification of cas no
The CAS Registry Mumber 4204-99-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,2,0 and 4 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 4204-99:
(6*4)+(5*2)+(4*0)+(3*4)+(2*9)+(1*9)=73
73 % 10 = 3
So 4204-99-3 is a valid CAS Registry Number.
InChI:InChI=1/C10H8FN3O2/c1-13-9(14(15)16)6-12-10(13)7-2-4-8(11)5-3-7/h2-6H,1H3
4204-99-3Relevant articles and documents
Process for preparing substituted nitroimidazoles
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, (2008/06/13)
2-(P-Fluorophenyl)-1-alkyl or 1-(2'-hydroxyalkyl)-5-nitroimidazoles are prepared by reacting a dialkoxy-carbonium salt, or a 1,3-dioxolenium salt, respectively, with 2-(p-fluorophenyl)-1-alkoxymethyl-4-nitroimidazole. The compounds prepared are useful in
