138175-25-4 Usage
Uses
Used in Pharmaceutical Synthesis:
2-Pyridinemethanamine, alpha-(1-methylethyl)-, (alphaR)-(9CI) is used as a key building block in the synthesis of pharmaceuticals for its ability to contribute to the development of new medications.
Used in Agrochemical Production:
In the agrochemical industry, 2-Pyridinemethanamine, alpha-(1-methylethyl)-, (alphaR)-(9CI) serves as an essential component in the creation of various agrochemicals, enhancing crop protection and yield.
Used in Organic Compound Synthesis:
2-Pyridinemethanamine,alpha-(1-methylethyl)-,(alphaR)-(9CI) is utilized as a versatile building block in the synthesis of a wide range of organic compounds, contributing to the advancement of organic chemistry.
Used in Antibiotic Development:
Due to its antimicrobial properties, 2-Pyridinemethanamine, alpha-(1-methylethyl)-, (alphaR)-(9CI) is used as a potential candidate in the development of new antibiotics, offering a novel approach to combat resistant bacterial strains.
Used in Antifungal Medication:
Leveraging its antifungal properties, 2-Pyridinemethanamine,alpha-(1-methylethyl)-,(alphaR)-(9CI) is explored for use in the development of new antifungal medications, addressing the need for effective treatments against fungal infections.
Check Digit Verification of cas no
The CAS Registry Mumber 138175-25-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,8,1,7 and 5 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 138175-25:
(8*1)+(7*3)+(6*8)+(5*1)+(4*7)+(3*5)+(2*2)+(1*5)=134
134 % 10 = 4
So 138175-25-4 is a valid CAS Registry Number.
138175-25-4Relevant academic research and scientific papers
An easy route to optically active 1-substituted-1-pyridyl-methylamines by diastereoselective reduction of enantiopure N-tert-butanesulfinyl ketimines
Chelucci, Giorgio,Baldino, Salvatore,Chessa, Simona,Pinna, Gerard A.,Soccolini, Franco
, p. 3163 - 3169 (2007/10/03)
The reduction of enantiopure N-tert-butanesulfinyl ketimines derived from pyridyl ketones afforded the related N-tert-butanesulfinyl amines with high yields and diastereoselectivities.
Asymmetric synthesis of 1-substituted-1-(pyridin-2-yl)methylamines by diastereoselective reduction of enantiopure N-p-toluenesulfinyl ketimines
Chelucci, Giorgio,Baldino, Salvatore,Solinas, Rosanna,Baratta, Walter
, p. 5555 - 5558 (2007/10/03)
Reduction of enantiopure N-p-toluenesulfinyl ketimines derived from 2-pyridyl ketones affords N-p-toluenesulfinyl amines with good yields and diastereoselectivities.
Asymmetric Synthesis XV: Enantioselective Syntheses of (R) or (S)-α-Substituted-(2-pyridyl) Methylamines via Chiral Pinanone Ketimine Template
Aiqiao, Mi,Xun, Xiao,Lanjun, Wu,Yaozhong, Jiang
, p. 2207 - 2212 (2007/10/02)
Enantioselective synthesis of (R) or (S)-α-substituted-(2-pyridyl)-methylamines (5), using 2-hydroxypinan-3-one (1) as chiral auxiliary, had been studied.The e.e. values of 5 were 89-98percent, which determined by chiral capillary GC (stationary phase; Chirasil-Val).
