138175-25-4 Usage
General Description
2-Pyridinemethanamine, alpha-(1-methylethyl)-, (alphaR)-(9CI) is a chemical compound with the molecular formula C8H12N2. It is a chiral molecule, with the (alphaR) enantiomer being the most stable form. 2-Pyridinemethanamine,alpha-(1-methylethyl)-,(alphaR)-(9CI) is often used in the synthesis of pharmaceuticals, agrochemicals, and other organic compounds. It can also be utilized as a building block in the production of various chemical intermediates. Additionally, it has been found to exhibit antimicrobial and antifungal properties, making it potentially useful in the development of new antibiotics or antifungal medications. Overall, 2-Pyridinemethanamine, alpha-(1-methylethyl)-, (alphaR)-(9CI) is a versatile compound with a range of potential applications in the field of chemistry and medicine.
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 articles and documents
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 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).
