871583-20-9 Usage
Uses
Used in Pharmaceutical Industry:
Methyl 4,6-dichloro-5-azaindole-2-carboxylate is used as a chemical intermediate for the synthesis of various biologically active compounds. Its heterocyclic structure and chlorinated nature contribute to the development of pharmaceutical products with therapeutic properties.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, Methyl 4,6-dichloro-5-azaindole-2-carboxylate is utilized as a building block in the creation of novel pharmaceutical agents. Its unique chemical properties allow for the design and synthesis of compounds with potential therapeutic applications.
Used in Drug Development:
Methyl 4,6-dichloro-5-azaindole-2-carboxylate plays a crucial role in drug development, as it is involved in the production of therapeutic compounds. Its potential applications in this area highlight its importance in the advancement of new treatments and medications.
Check Digit Verification of cas no
The CAS Registry Mumber 871583-20-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,1,5,8 and 3 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 871583-20:
(8*8)+(7*7)+(6*1)+(5*5)+(4*8)+(3*3)+(2*2)+(1*0)=189
189 % 10 = 9
So 871583-20-9 is a valid CAS Registry Number.
InChI:InChI=1/C9H6Cl2N2O2/c1-15-9(14)6-2-4-5(12-6)3-7(10)13-8(4)11/h2-3,12H,1H3
871583-20-9Relevant academic research and scientific papers
The Hemetsberger-Knittel synthesis of substituted 5-, 6-, and 7-azaindoles
Roy, Patrick J.,Dufresne, Claude,Lachance, Nicolas,Leclerc, Jean-Philippe,Boisvert, Michel,Wang, Zhaoyin,Leblanc, Yves
, p. 2751 - 2757 (2007/10/03)
A series of substituted 5-, 6-, and 7-azaindoles were prepared via the Hemetsberger-Knittel reaction. In general, better yields were obtained at higher temperatures and shorter reaction times than required for the formation of the analogous indoles, and in some cases, only decomposition occurred below a minimum temperature. The resulting templates offer up to five sites for subsequent functionalization to allow a wide range of chemical diversity. Georg Thieme Verlag Stuttgart.
