84483-27-2 Usage
General Description
2-BROMO-6-IODOANILINE is a chemical compound that consists of a benzene ring with a bromine atom at the 2 position and an iodine atom at the 6 position. It is classified as an aniline derivative, which is a type of aromatic amine. 2-BROMO-6-IODOANILINE is commonly used in organic synthesis and as a building block in the production of various pharmaceuticals and agrochemicals. It has also been utilized in the synthesis of dyes and pigments due to its ability to undergo various chemical reactions. Additionally, 2-BROMO-6-IODOANILINE has been studied for its potential biological activities and has shown to possess antimicrobial and antitumor properties, making it a subject of interest in medicinal chemistry research.
Check Digit Verification of cas no
The CAS Registry Mumber 84483-27-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,4,4,8 and 3 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 84483-27:
(7*8)+(6*4)+(5*4)+(4*8)+(3*3)+(2*2)+(1*7)=152
152 % 10 = 2
So 84483-27-2 is a valid CAS Registry Number.
84483-27-2Relevant articles and documents
A dramatic enhancing effect of InBr3 towards the oxidative Sonogashira cross-coupling reaction of 2-ethynylanilines
Ikeda,Omote,Kusumoto,Komori,Tarui,Sato,Ando
supporting information, p. 2127 - 2133 (2016/02/18)
The addition of InBr3 to the oxidative Sonogashira cross-coupling reaction of 2-ethynylaniline with (E)-trimethyl(3,3,3-trifluoroprop-1-enyl)silane led to a dramatic increase in the reactivity to afford the corresponding 1,3-enynes bearing a trifluoromethyl group on their terminal sp2 carbon. The subsequent cyclization of these 1,3-enynes under palladium catalysis provides access to the corresponding indoles bearing a 3,3,3-trifluoroprop-1-enyl group at their 2-position.
Synthesis of pyrrolnitrin and related halogenated phenylpyrroles
Morrison, Matthew D.,Hanthorn, Jason J.,Pratt, Derek A.
supporting information; experimental part, p. 1051 - 1054 (2009/07/18)
A general approach to halogenated arylpyrroles, including the antifungal natural product pyrrolnitrin, is described using newly synthesized halogenated pyrroles and 2,6-disubstituted nitrobenzenes or 2,6-disubstituted anilines.
