55270-27-4 Usage
Uses
Used in Organic Synthesis:
4-Bromoisoquinolin-1-amine is utilized as a key intermediate in organic synthesis for the preparation of a variety of biologically active compounds. Its reactivity and structural features facilitate the synthesis of complex organic molecules that can be further modified for specific applications.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, 4-bromoisoquinolin-1-amine is employed as a building block for the development of new drugs. Its unique chemical properties allow for the design of molecules with potential therapeutic effects, contributing to the advancement of pharmaceutical research and drug discovery.
Used in Materials Science:
4-Bromoisoquinolin-1-amine has potential applications in materials science, where its chemical properties can be harnessed to create new materials with specific characteristics. This can include the development of materials with tailored electronic, optical, or mechanical properties.
Used in Catalysis:
4-bromoisoquinolin-1-amine also finds use in catalysis, where its reactivity can be exploited to facilitate chemical reactions. This can lead to more efficient and selective catalytic processes, which are crucial in various industrial applications and chemical transformations.
Check Digit Verification of cas no
The CAS Registry Mumber 55270-27-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,2,7 and 0 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 55270-27:
(7*5)+(6*5)+(5*2)+(4*7)+(3*0)+(2*2)+(1*7)=114
114 % 10 = 4
So 55270-27-4 is a valid CAS Registry Number.
55270-27-4Relevant academic research and scientific papers
Electrochemical C-H Halogenations of Enaminones and Electron-Rich Arenes with Sodium Halide (NaX) as Halogen Source for the Synthesis of 3-Halochromones and Haloarenes
Lin, Yan,Jin, Jun,Wang, Chaoli,Wan, Jie-Ping,Liu, Yunyun
, p. 12378 - 12385 (2021/09/07)
Without employing an external oxidant, the simple synthesis of 3-halochromones and various halogenated electron-rich arenes has been realized with electrode oxidation by employing the simplest sodium halide (NaX, X = Cl, Br, I) as halogen source. This electrochemical method is advantageous for the simple and mild room temperature operation, environmental friendliness as well as broad substrate scope in both C-H bond donor and halogen source components.
Synthesis and reactions of some heterocyclic azacyanines
Huang,Haddadin,Olmstead,Kurth
, p. 1310 - 1315 (2007/10/03)
The one-step reaction of some amino-substituted heterocycles with diiodomethane to give azacyanines is reported. This useful reaction is of wider application than initially reported and includes the synthesis of new substituted pyrido-, isoquino-, benzimadazo-, and benzothiazoazacyanines 7. Furthermore, treatment of these azacyanines with base generally affects a facile opening of the dihydrotriazinium ring resulting in the formation of new heterocycles 10, 11, and 12, which would be difficult to prepare by other means. This reaction takes an additional direction in the case of halo-substituted azacyanines 7b/c/d where treatment with base gives rise to new interesting derivatives of dipyridotriazines 14b/c/d.
