1086389-94-7 Usage
Description
3,5-DibroMo-1H-pyrrolo[2,3-b]pyridine is a brominated heterocyclic compound with the molecular formula C7H4Br2N2. It features a pyrrolopyridine ring system and is known for its potential applications in pharmaceuticals and agrochemicals due to its unique structure and properties. 3,5-DibroMo-1H-pyrrolo[2,3-b]pyridine can also serve as a building block in organic synthesis for creating more complex molecules. However, it is crucial to handle 3,5-DibroMo-1H-pyrrolo[2,3-b]pyridine with care due to its potential health and environmental hazards.
Uses
Used in Pharmaceutical Industry:
3,5-DibroMo-1H-pyrrolo[2,3-b]pyridine is used as a chemical intermediate for the development of new pharmaceutical compounds. Its unique structure allows it to be a promising candidate in the synthesis of drugs with specific therapeutic properties.
Used in Agrochemical Industry:
In the agrochemical sector, 3,5-DibroMo-1H-pyrrolo[2,3-b]pyridine is utilized as a starting material for the synthesis of agrochemicals, such as pesticides and herbicides. Its brominated heterocyclic nature contributes to the effectiveness of these products in controlling pests and weeds.
Used in Organic Synthesis:
3,5-DibroMo-1H-pyrrolo[2,3-b]pyridine is used as a building block in organic synthesis for creating more complex molecules with diverse applications. Its pyrrolopyridine ring system provides a foundation for the development of advanced chemical compounds with specific functions and properties.
Check Digit Verification of cas no
The CAS Registry Mumber 1086389-94-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,8,6,3,8 and 9 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1086389-94:
(9*1)+(8*0)+(7*8)+(6*6)+(5*3)+(4*8)+(3*9)+(2*9)+(1*4)=197
197 % 10 = 7
So 1086389-94-7 is a valid CAS Registry Number.
1086389-94-7Relevant articles and documents
Regioselective Halogenation of Arenes and Heterocycles in Hexafluoroisopropanol
Tang, Ren-Jin,Milcent, Thierry,Crousse, Benoit
, p. 930 - 938 (2018/01/28)
Regioselective halogenation of arenes and heterocycles with N-halosuccinimides in fluorinated alcohols is disclosed. Under mild condition reactions, a wide diversity of halogenated arenes are obtained in good yields with high regioselectivity. Additionally, the versatility of the method is demonstrated by the development of one-pot sequential halogenation and halogenation-Suzuki cross-coupling reactions.
