1132940-43-2 Usage
Benzene derivative
As a derivative of benzene, 1-tert-butyl-3-iodo-2-methoxy-5-nitrobenzene has a benzene ring as its central structure, with various substituents attached to it.
tert-Butyl group
C4H9 A tert-butyl group is attached to the benzene ring, which is an alkyl group with four carbon atoms and a tertiary carbon center.
Iodine atom
I An iodine atom is attached to the benzene ring, which is a halogen with 53 protons and 74 neutrons in its nucleus.
Methoxy group
OCH3 A methoxy group is attached to the benzene ring, which is an ether functional group consisting of an oxygen atom bonded to a methyl group (CH3).
Nitro group
NO2 A nitro group is attached to the benzene ring, which is a functional group consisting of an oxygen atom double-bonded to a nitrogen atom.
Organic synthesis reagent
1-tert-butyl-3-iodo-2-methoxy-5-nitrobenzene is commonly used in organic synthesis as a reagent for introducing an iodine atom into other molecules.
Pharmaceutical industry application
It is used in the pharmaceutical industry for the development of new drugs, thanks to its unique chemical properties.
Agrochemical production
The compound is also used in the production of agrochemicals, which are chemicals used to enhance crop productivity and control pests.
Unique chemical properties
The presence of both the methoxy and nitro groups in its structure gives 1-tert-butyl-3-iodo-2-methoxy-5-nitrobenzene unique chemical properties, making it suitable for various applications in different fields.
Check Digit Verification of cas no
The CAS Registry Mumber 1132940-43-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,3,2,9,4 and 0 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1132940-43:
(9*1)+(8*1)+(7*3)+(6*2)+(5*9)+(4*4)+(3*0)+(2*4)+(1*3)=122
122 % 10 = 2
So 1132940-43-2 is a valid CAS Registry Number.
1132940-43-2Relevant academic research and scientific papers
Synthesis and Biological Characterization of Aryl Uracil Inhibitors of Hepatitis C Virus NS5B Polymerase: Discovery of ABT-072, a trans-Stilbene Analog with Good Oral Bioavailability
Randolph, John T.,Krueger, A. Chris,Donner, Pamela L.,Pratt, John K.,Liu, Dachun,Motter, Christopher E.,Rockway, Todd W.,Tufano, Michael D.,Wagner, Rolf,Lim, Hock B.,Beyer, Jill M.,Mondal, Rubina,Panchal, Neeta S.,Colletti, Lynn,Liu, Yaya,Koev, Gennadiy,Kati, Warren M.,Hernandez, Lisa E.,Beno, David W. A.,Longenecker, Kenton L.,Stewart, Kent D.,Dumas, Emily O.,Molla, Akhteruzzaman,Maring, Clarence J.
, p. 1153 - 1163 (2018/02/17)
ABT-072 is a non-nucleoside HCV NS5B polymerase inhibitor that was discovered as part of a program to identify new direct-acting antivirals (DAAs) for the treatment of HCV infection. This compound was identified during a medicinal chemistry effort to impr
ANTI-INFECTIVE PYRIMIDINES AND USES THEREOF
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Page/Page column 98-99; 108, (2009/04/25)
This invention relates to: (a) compounds and salts thereof that, inter alia, inhibit HCV; (b) intermediates useful for the preparation of such compounds and salts; (c) compositions comprising such compounds and salts; (d) methods for preparing such intermediates, compounds, salts, and compositions; (e) methods of use of such compounds, salts, and compositions; and (f) kits comprising such compounds, salts, and compositions.
