64138-65-4 Usage
Uses
Used in Pharmaceutical Synthesis:
(R)-(+)-2-(ALPHA-METHYLBENZYLAMINO)-5-NITROPYRIDINE is used as a building block in pharmaceutical synthesis for the development of new drug compounds. Its unique structure and chirality make it a promising candidate for creating innovative and effective medications.
Used in Pesticidal Activities:
In the agricultural industry, (R)-(+)-2-(ALPHA-METHYLBENZYLAMINO)-5-NITROPYRIDINE is used as a potential active ingredient in pesticides. Its pesticidal properties are currently under investigation, with the aim of developing more effective and environmentally friendly pest control solutions.
Used in Industrial Applications:
(R)-(+)-2-(ALPHA-METHYLBENZYLAMINO)-5-NITROPYRIDINE is also being explored for its potential use in various industrial applications. Its unique chemical structure and properties may offer advantages in the development of new materials, processes, or products across different sectors.
Check Digit Verification of cas no
The CAS Registry Mumber 64138-65-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,4,1,3 and 8 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 64138-65:
(7*6)+(6*4)+(5*1)+(4*3)+(3*8)+(2*6)+(1*5)=124
124 % 10 = 4
So 64138-65-4 is a valid CAS Registry Number.
64138-65-4Relevant 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.
