89466-17-1 Usage
Description
6-Bromo-5-methyl-2-pyridinamine, with the chemical formula C6H7BrN2, is an organic compound that appears as a white to light brown solid. It is primarily recognized for its role as an intermediate in the synthesis of pharmaceuticals and agrochemicals. Known by its CAS number 25332-30-3, this compound is utilized in the production of a variety of chemical products. Due to its potential hazards upon ingestion, inhalation, or skin contact, it is crucial to handle and store 6-Bromo-5-methyl-2-pyridinamine with care, keeping it in a cool, dry environment away from direct sunlight and heat sources.
Uses
Used in Pharmaceutical Industry:
6-Bromo-5-methyl-2-pyridinamine is used as a chemical intermediate for the synthesis of various pharmaceuticals. It plays a crucial role in the development of new drugs, contributing to the advancement of medicinal chemistry.
Used in Agrochemical Industry:
In the agrochemical sector, 6-Bromo-5-methyl-2-pyridinamine is employed as an intermediate in the production of agrochemicals. It aids in the creation of compounds that can enhance crop protection and contribute to sustainable agriculture practices.
Used in Chemical Product Manufacturing:
6-Bromo-5-methyl-2-pyridinamine is utilized in the manufacturing of a range of chemical products. Its versatility as an intermediate allows for its incorporation into multiple chemical formulations, expanding its applications across various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 89466-17-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,4,6 and 6 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 89466-17:
(7*8)+(6*9)+(5*4)+(4*6)+(3*6)+(2*1)+(1*7)=181
181 % 10 = 1
So 89466-17-1 is a valid CAS Registry Number.
89466-17-1Relevant articles and documents
Technological method for preparing 2- amino -6-5-methyl-substituted-pyridine (by machine translation)
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Paragraph 0061-0085, (2020/01/12)
The reaction solvent of 2 - the method is reacted in a reaction solvent under the action, of 2 - an, acid anhydride and an acid,binding, agent and an amination reagent under the action. of an acid anhydride and 2 - an acid-binding agent and, an amination reagent, 2 -4 - 93/7, 99.8%, 70%. (by machine translation)
SOLID FORMS OF LUMACAFTOR, ITS SALTS AND PROCESSES THEREOF
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, (2017/11/04)
Aspects of the present application relate to solid forms of Lumacaftor, its salts and processes thereof. Specific aspects of the present application relate to alternate processes for the preparation of Lumacaftor and intermediates thereof. Present application further relates to the solid forms of Lumacaftor and its salts.
Synthesis of 5-bromo-6-methyl imidazopyrazine, 5-bromo and 5-chloro-6-methyl imidazopyridine using electron density surface maps to guide synthetic strategy
Harris, Anthony R.,Nason, Deane M.,Collantes, Elizabeth M.,Xu, Wenjian,Chi, Yushi,Wang, Zhihan,Zhang, Bingzhi,Zhang, Qingjian,Gray, David L.,Davoren, Jennifer E.
experimental part, p. 9063 - 9066 (2011/12/03)
Small heteroaromatic rings are valuable monomers in drug discovery that can enable rapid access to novel and desirable chemical space. Installation of a synthetic handle on a heteroaromatic core may be difficult if steric and electronic factors are not in alignment with the desired transformation. Described are practical routes for the construction of 5-bromo-6-methyl imidazopyrazine (1) as well as 5-bromo and 5-chloro-6-methyl imidazopyridines (2a and 2b), which were developed using electron density surface maps encoded with ionization potential to guide synthetic strategy.
