400877-05-6 Usage
Description
4-Aminomethyl-1-methylpyrazole, also known as AMP, is a heterocyclic organic compound characterized by a molecular formula of C5H8N2. It features a pyrazole ring with an amino group attached to a methyl group, making it a versatile chemical entity in various scientific and industrial applications.
Uses
Used in Coordination Chemistry:
4-Aminomethyl-1-methylpyrazole is used as a ligand for its ability to coordinate with metal ions, facilitating the formation of stable complexes in coordination chemistry.
Used in Metal-Ion Transport:
AMP is used as a chelating agent in metal-ion transport, where its ability to bind metal ions aids in their movement and management within chemical systems.
Used in Pharmaceutical Synthesis:
4-Aminomethyl-1-methylpyrazole is used as a key component in the synthesis of various pharmaceutical compounds, contributing to the development of new drugs and therapies.
Used as a Reagent in Organic Chemistry:
AMP serves as a reagent in organic chemistry reactions, where its unique structure and functional groups participate in a range of chemical transformations.
Used in Disease Treatment Research:
4-Aminomethyl-1-methylpyrazole has been studied for its potential application in the treatment of various diseases, indicating its possible role in medical research and development.
Used as an Enzyme Inhibitor:
AMP is also considered for its capacity to inhibit specific enzymes, which can be crucial in controlling enzymatic activity related to certain pathological conditions or in the development of enzyme-targeted drugs.
Check Digit Verification of cas no
The CAS Registry Mumber 400877-05-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,0,0,8,7 and 7 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 400877-05:
(8*4)+(7*0)+(6*0)+(5*8)+(4*7)+(3*7)+(2*0)+(1*5)=126
126 % 10 = 6
So 400877-05-6 is a valid CAS Registry Number.
InChI:InChI=1/C5H9N3/c1-8-4-5(2-6)3-7-8/h3-4H,2,6H2,1H3
400877-05-6Relevant articles and documents
Efficient hydrogenation of benzaldoximes and Schiff bases on ceramic high-porosity palladium catalysts
Ignatov,Varakutin,Solov’eva,Karmanova,Kozlov,Semenova,Semenov
, p. 1394 - 1400 (2018/10/31)
An efficient catalytic method for the synthesis of benzyl- and dibenzylamines by hydrogenating oximes and Schiffbases was developed on palladium supported high-porosity foamed ceramic block catalyst. The multiple regeneration ability of the foamed ceramic block catalyst can significantly decrease the Pd consumption as compared to the use of the conventional 10%Pd/C catalyst. Owing to a high hardness of the foamed ceramic catalyst, the reaction mixture can rapidly be removed from the reactor without using filtering devices. The structures produced by the reaction are fragments of biologically active and natural molecules. Antiproliferative properties of dibenzylamines revealed on the sea urchin embryo model suggest that these compounds can be considered as promising agents for the design of new anticancer drugs.
