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69214-12-6

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69214-12-6 Usage

General Description

3,5-Dibromomidazo[1,2-a]pyridine is a chemical compound with the molecular formula C7H5Br2N3. It is a heterocyclic compound containing a pyridine ring fused to an imidazo ring with bromine atoms attached at the 3 and 5 positions. This chemical is a building block in organic synthesis and can be used in the preparation of various pharmaceutical and agrochemical products. It is often used as a reagent in the creation of diverse chemical compounds due to its versatile reactivity and ability to participate in various organic reactions. Additionally, it has the potential to exhibit biological activity and may have applications in medicinal research and drug discovery.

Check Digit Verification of cas no

The CAS Registry Mumber 69214-12-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,2,1 and 4 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 69214-12:
(7*6)+(6*9)+(5*2)+(4*1)+(3*4)+(2*1)+(1*2)=126
126 % 10 = 6
So 69214-12-6 is a valid CAS Registry Number.
InChI:InChI=1/C7H4Br2N2/c8-5-2-1-3-7-10-4-6(9)11(5)7/h1-4H

69214-12-6Downstream Products

69214-12-6Relevant articles and documents

peri-Substituted Imidazopyridines. A New Reductive Elimination Reaction

Rees, Charles W.,Smith, David I.

, p. 1159 - 1164 (2007/10/02)

A new reductive elimination reaction of 3,5-disubstituted imidazopyridines (3) with hydrazine is reported.Thus on treatment of the 3,5-dibromo (7a), 5-bromo-3-nitro (7b), and 3,5-dinitro (4) derivatives with hydrazine hydrate in hot ethanol, the bromine and nitro groups are replaced by hydrogen.A mechanism based on the conjugated relationship of these peri-substituents is proposed and used to explain the reported conversion of 1,3,5-trichloro-2,4,6-trinitrobenzene (9) into 1,3-dichloro-4,6-dinitrobenzene (10).A variety of other 3-nitro-5-substituted imidazopyridines (15)-(18) is described, but these could not be cyclised to 1,2,4-triazacyclopentindenes.The 3-amino-5-methoxycarbonyl derivative (19a) cyclises to the triazacyclopentindenone (20) with sodium methoxide.

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