289038-12-6 Usage
General Description
2-Bromo-4-methyl-6-iodoaniline is a chemical compound with the molecular formula C7H8BrIN. It is a substituted aniline derivative, consisting of a benzene ring with a bromine atom in the 2 position, a methyl group in the 4 position, and an iodine atom in the 6 position. 2-BROMO-4-METHYL-6-IODOANILINE is commonly used as an intermediate in the synthesis of pharmaceuticals, dyes, and agrochemicals. It has also been studied for its potential use as a building block in organic synthesis and pharmaceutical development. The chemical properties and reactivity of 2-Bromo-4-methyl-6-iodoaniline make it a valuable ingredient for various industrial and research applications.
Check Digit Verification of cas no
The CAS Registry Mumber 289038-12-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,8,9,0,3 and 8 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 289038-12:
(8*2)+(7*8)+(6*9)+(5*0)+(4*3)+(3*8)+(2*1)+(1*2)=166
166 % 10 = 6
So 289038-12-6 is a valid CAS Registry Number.
289038-12-6Relevant articles and documents
Phenanthridine-Containing Pincer-like Amido Complexes of Nickel, Palladium, and Platinum
Mandapati, Pavan,Giesbrecht, Patrick K.,Davis, Rebecca L.,Herbert, David E.
, p. 3674 - 3685 (2017/03/24)
Proligands based on bis(8-quinolinyl)amine (L1) were prepared containing one (L2) and two (L3) benzo-fused N-heterocyclic phenanthridinyl (3,4-benzoquinolinyl) units. Taken as a series, L1-L3 provides a ligand template for exploring systematic π-extension
Asymmetric radical and anionic cyclizations of axially chiral carbamates
Guthrie, David B.,Curran, Dennis P.
supporting information; experimental part, p. 249 - 251 (2009/06/28)
Standard Boc, Alloc, and Cbz derivatives of N-2,4-dimethyl-6-iodophenyl-N- allyl anilines are axially chiral and can be readily resolved into atropisomers whose racemization barriers exceed 30 kcal/mol. The resolved axially chiral carbamates undergo radic