84249-39-8 Usage
Uses
Since the provided materials do not specify the exact applications of (S)-(-)-2-(ALPHA-METHYLBENZYLAMINO)-5-NITROPYRIDINE, it is not possible to list its uses as in the example of Gallotannin. However, based on its chemical structure and properties, potential applications could include:
Used in Pharmaceutical Industry:
(S)-(-)-2-(ALPHA-METHYLBENZYLAMINO)-5-NITROPYRIDINE could be used as an intermediate or active ingredient in the development of pharmaceutical compounds, due to its unique combination of amino, nitro, and aromatic functionalities, which may allow for specific interactions with biological targets.
Used in Chemical Research:
(S)-(-)-2-(ALPHA-METHYLBENZYLAMINO)-5-NITROPYRIDINE could be used as a research tool in the study of chiral chemistry, stereochemistry, and the development of new synthetic methods or reactions that involve its unique structural features.
Used in Material Science:
(S)-(-)-2-(ALPHA-METHYLBENZYLAMINO)-5-NITROPYRIDINE's structural properties might also make it a candidate for use in the development of new materials with specific properties, such as in the fields of catalysis or as a component in the synthesis of advanced materials.
Check Digit Verification of cas no
The CAS Registry Mumber 84249-39-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,4,2,4 and 9 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 84249-39:
(7*8)+(6*4)+(5*2)+(4*4)+(3*9)+(2*3)+(1*9)=148
148 % 10 = 8
So 84249-39-8 is a valid CAS Registry Number.
84249-39-8Relevant academic research and scientific papers
Diacylglycerol acyltransferase inhibitors
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Page/Page column 20, (2010/11/27)
Provided herein are compounds of the formula (I): as well as pharmaceutically acceptable salts thereof, wherein the substituents are as those disclosed in the specification. These compounds, and the pharmaceutical compositions containing them, are useful for the treatment of diseases such as, for example, obesity, type II diabetes mellitus and metabolic syndrome.
Substitution reactions of 5-nitropyridine-2-sulfonic acid. A new pathway to 2,5-disubstituted pyridines
Bakke, Jan M.,Sletvold, Ingrid
, p. 2710 - 2715 (2007/10/03)
We have investigated reactions of 5-nitropyridine-2-sulfonic acid and its potassium salt in which substitution of the sulfonate group by oxygen, nitrogen and halogen nucleophiles has been attempted. By this approach, 2-methoxy-(95% yield), 2-ethoxy- (97%), 2-isopropoxy- (65%), 2-amino- (92%), 2- butylamino- (76%), 2-diethylamino- (62%), 2-ethylamino- (32%), 2-benzylamino- (77%), 2-(R-1-phenylethylamino)- (71%) and 2-chloro-5-nitropyridine (87%) have been obtained. No reactions were observed with phenols or anilines. With t-BuOH, 2-hydroxy-5-nitropyridine was formed together with 2-methylpropene.
