1000017-92-4 Usage
Uses
Used in Pharmaceutical Industry:
2-Chloro-3,5-dibromo-4-methylpyridine is used as an intermediate in the synthesis of various pharmaceutical compounds for its unique reactivity and functional groups. Its presence in the molecular structure can influence the properties and efficacy of the final drug products.
Used in Organic Synthesis:
In the field of organic synthesis, 2-Chloro-3,5-dibromo-4-methylpyridine serves as a key building block for the creation of complex organic molecules. Its distinct substituent groups allow for versatile chemical reactions, facilitating the development of novel compounds with potential applications in various industries.
Safety Precautions:
As with many organic chemicals, it is crucial to follow safety precautions while handling 2-Chloro-3,5-dibromo-4-methylpyridine to minimize potential health hazards. Proper protective equipment, controlled environments, and adherence to safety guidelines are essential to ensure the safe use of this compound in research and industrial applications.
Check Digit Verification of cas no
The CAS Registry Mumber 1000017-92-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,0,0,0,1 and 7 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1000017-92:
(9*1)+(8*0)+(7*0)+(6*0)+(5*0)+(4*1)+(3*7)+(2*9)+(1*2)=54
54 % 10 = 4
So 1000017-92-4 is a valid CAS Registry Number.
InChI:InChI=1/C6H4Br2ClN/c1-3-4(7)2-10-6(9)5(3)8/h2H,1H3
1000017-92-4Relevant articles and documents
Iron(II)-Based Metalloradical Activation: Switch from Traditional Click Chemistry to Denitrogenative Annulation
Roy, Satyajit,Khatua, Hillol,Das, Sandip Kumar,Chattopadhyay, Buddhadeb
supporting information, p. 11439 - 11443 (2019/07/17)
A unique concept for the intermolecular denitrogenative annulation of 1,2,3,4-tetrazoles and alkynes was discovered by using a catalytic amount of Fe(TPP)Cl and Zn dust. The reaction precludes the traditional, more favored click reaction between an organic azide and alkynes, and instead proceeds by an unprecedented metalloradical activation. The method is anticipated to advance access to the construction of important basic nitrogen heterocycles, which will in turn enable discoveries of new drug candidates.
