1070879-23-0 Usage
General Description
4-Bromo-6-methylquinoline is a chemical compound with the molecular formula C10H8BrN. It is a heterocyclic compound containing a quinoline ring with a bromine atom at the 4-position and a methyl group at the 6-position. 4-Bromo-6-methylquinoline is used in the pharmaceutical industry as an intermediate for the synthesis of various biologically active compounds, including potential drug candidates. It is also used in research and development, particularly in the study of organic synthesis and the development of new chemical reactions. 4-Bromo-6-methylquinoline is considered to be a versatile building block for the preparation of a wide range of functionalized quinoline derivatives with potential applications in medicinal chemistry and drug discovery.
Check Digit Verification of cas no
The CAS Registry Mumber 1070879-23-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,7,0,8,7 and 9 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1070879-23:
(9*1)+(8*0)+(7*7)+(6*0)+(5*8)+(4*7)+(3*9)+(2*2)+(1*3)=160
160 % 10 = 0
So 1070879-23-0 is a valid CAS Registry Number.
1070879-23-0Relevant articles and documents
A highly practical and convenient halogenation of fused heterocyclic N-oxides
Wang, Dong,Wang, Yuxi,Zhao, Junjie,Li, Linna,Miao, Longfei,Wang, Dong,Sun, Hua,Yu, Peng
, p. 5762 - 5768 (2016/08/30)
A novel, simple and practical method for the regioselective halogenation of fused heterocyclic N-oxides has been developed. It employs Vilsmeier reagent, generated in situ by POX3and DMF, as both the activating agent and the nucleophilic halide source. The method is amenable across a broad range of substrates, including quinolines, isoquinolines and the diazine N-oxides, possessing a variety of substitution patterns. Furthermore, all of the reagents associated are cheap and easy to obtain. The potential extension of this method to a one-pot oxidation/halogenation sequence that obviates the need for isolation of the N-oxide intermediates is also presented.
