141278-22-0 Usage
General Description
1H-Indazole-1-ethanol, 3-chloro-a-(chloromethyl)-5-nitro- is a chemical compound with the molecular formula C10H9Cl2N3O3. It is a nitro-substituted derivative of indazole ethanol, which is a class of compounds known for their diverse pharmacological activities. This specific compound is characterized by the presence of a 3-chloro-a-(chloromethyl) group and a 5-nitro group, which may impart specific reactivity and properties. The compound's structure suggests potential applications in medicinal chemistry, as nitro and chloromethyl groups are common functional groups in pharmacologically active compounds. Additionally, the presence of an indazole moiety in its structure indicates possible bioactivity and could warrant further investigation for its potential biological and pharmacological properties.
Check Digit Verification of cas no
The CAS Registry Mumber 141278-22-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,1,2,7 and 8 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 141278-22:
(8*1)+(7*4)+(6*1)+(5*2)+(4*7)+(3*8)+(2*2)+(1*2)=110
110 % 10 = 0
So 141278-22-0 is a valid CAS Registry Number.
141278-22-0Relevant articles and documents
Azoles. Part 32: Nitroindazole derivatives and their electron affinity
Usarewicz,Wrzeciono,Lukaszewski,Gatniejewska,Peisert
, p. 15 - 18 (2007/10/02)
A modified procedure for the synthesis of the dinitroindazoles 5-8 is described. Treatment of the chloronitro- and dinitroindazoles 1-8 with epichlorohydrin afforded the chlorohydroxypropyl- and epoxypropylindazole derivatives 2a-8a, 1b-5b, 7b and 7c. The structure of the compounds is confirmed by the aid of their IR, 1H and 13C NMR spectra. The electron affinity of the nitroindazole derivatives 1-16 is discussed on the basis of their halfwave potentials and in the combination with their eventual radiosensitizing properties.
