28036-33-1 Usage
Description
3-AMINOIMIDAZO(1,2-A)PYRIDINE is a chemical compound that serves as an intermediate in the synthesis of various mutagenic pyrolyzates. It is a heterocyclic compound with a nitrogen-containing ring structure, which contributes to its mutagenic properties.
Uses
Used in Chemical Synthesis:
3-AMINOIMIDAZO(1,2-A)PYRIDINE is used as an intermediate in the production of mutagenic pyrolyzates for various applications in the chemical industry. Its unique chemical structure allows it to be a key component in the synthesis of these compounds, which can be further utilized in research and development.
Used in Research and Development:
In the field of research and development, 3-AMINOIMIDAZO(1,2-A)PYRIDINE is used as a starting material for the creation of new mutagenic pyrolyzates. These compounds can be studied for their potential applications in various scientific and industrial processes, including genetic research and the development of new materials with specific properties.
Used in Pharmaceutical Industry:
Although not explicitly mentioned in the provided materials, 3-AMINOIMIDAZO(1,2-A)PYRIDINE may also have potential applications in the pharmaceutical industry. Its mutagenic properties could be of interest for researchers working on the development of new drugs or therapies, particularly those focused on genetic manipulation or targeted cancer treatments. However, further research and development would be necessary to explore these potential applications fully.
Check Digit Verification of cas no
The CAS Registry Mumber 28036-33-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,8,0,3 and 6 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 28036-33:
(7*2)+(6*8)+(5*0)+(4*3)+(3*6)+(2*3)+(1*3)=101
101 % 10 = 1
So 28036-33-1 is a valid CAS Registry Number.
InChI:InChI=1/C7H7N3/c8-6-5-9-7-3-1-2-4-10(6)7/h1-5H,8H2
28036-33-1Relevant articles and documents
Structure-Function Evaluation of Imidazopyridine Derivatives Selective for δ-Subunit-Containing γ-Aminobutyric Acid Type A (GABAA) Receptors
Yakoub, Kirsten,Jung, Sascha,Sattler, Christian,Damerow, Helen,Weber, Judith,Kretzschmann, Annika,Cankaya, Aylin S.,Piel, Markus,R?sch, Frank,Haugaard, Anne S.,Fr?lund, Bente,Schirmeister, Tanja,Lüddens, Hartmut
, p. 1951 - 1968 (2018/03/21)
δ-Selective compounds 1 and 2 (DS1, compound 22; DS2, compound 16) were introduced as functionally selective modulators of δ-containing GABA type A receptors (GABAAR). In our hands, [3H]EBOB-binding experiments with recombinant GABAAR and compound 22 showed no proof of δ-selectivity, although there was a minimally higher preference for the α4β3δ and α6β2/3δ receptors with respect to potency. In order to delineate the structural determinants of δ preferences, we synthesized 25 derivatives of DS1 and DS2, and investigated their structure-activity relationships (SAR). Four of our derivatives showed selectivity for α6β3δ receptors (29, 38, 39, and 41). For all of them, the major factors that distinguished them from compound 22 were variations at the para-positions of their benzamide groups. However, two compounds (29 and 39), when tested in the presence of GABA, revealed effects at several additional GABAAR. The newly synthesized compounds will still serve as useful tools to investigate α6β3δ receptors.
Studies on Heterocyclic Compounds: Part I. Synthesis of 3-amino-2-sub-Imidazo(1,2-a)-pyridines
Astik, R. R.,Thaker, K. A.
, p. 1013 - 1014 (2007/10/02)
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