127915-47-3 Usage
Uses
Used in Pharmaceutical Industry:
Ethanone,1-(4-amino-6-methyl-3-pyridinyl)is used as a key intermediate in the synthesis of various pharmaceuticals for its ability to form complex molecular structures. Its presence in the molecular composition of drugs contributes to their therapeutic effects and medicinal properties.
Used in Agricultural Chemical Industry:
In the agricultural sector, Ethanone,1-(4-amino-6-methyl-3-pyridinyl)is utilized as a precursor in the production of agricultural chemicals. Its unique chemical structure allows for the development of effective compounds that can be used in crop protection and pest control.
Used in Organic Chemistry Research:
As a versatile building block, Ethanone,1-(4-amino-6-methyl-3-pyridinyl)is employed in organic chemistry research for the synthesis of new organic compounds. Its reactivity and functional groups enable the creation of a wide range of molecules with potential applications in various fields.
Used in the Production of Biologically Active Molecules:
Ethanone,1-(4-amino-6-methyl-3-pyridinyl)is used as a starting material in the synthesis of biologically active molecules. Its unique structure allows for the development of compounds with specific biological activities, making it a valuable asset in the discovery and production of new therapeutic agents and other bioactive substances.
Check Digit Verification of cas no
The CAS Registry Mumber 127915-47-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,7,9,1 and 5 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 127915-47:
(8*1)+(7*2)+(6*7)+(5*9)+(4*1)+(3*5)+(2*4)+(1*7)=143
143 % 10 = 3
So 127915-47-3 is a valid CAS Registry Number.
127915-47-3Relevant articles and documents
Improved Synthesis of N1-Pyridylthiamine Pyrophosphate, a Coenzymatically Active Analog of Thiamine Pyrophosphate
Neef, Holger,Golbik, Ralph,Fahlbusch, Baerbel,Schellenberger, Alfred
, p. 913 - 916 (2007/10/02)
Our previously published synthesis of the N1-pyridyl analog 1b of thiamine pyrophosphate is improved resulting in a remarkably higher yield.Key reaction of this new synthetic pathway is the oxidative degradation of 5-acetylpyridine 8 to the 5-carboxylic acid 11 via the pyridinium compound 10.Improved preparations of other intermediates are also described.The N1-pyridylthiamine pyrophosphate analog 1b has been separated and purified by ion exchange chromatography on Sephadex A-25.