144852-40-4

Basic information

• Product Name: (S)-3-methyl-1-(pyridin-2-yl)butan-1-amine
• CAS NO: 144852-40-4
• Molecular Weight: 164.25
• Mol File: 144852-40-4.mol

Chemical Properties

• CAS DataBase Reference: (S)-3-methyl-1-(pyridin-2-yl)butan-1-amine(CAS DataBase Reference)
• NIST Chemistry Reference: (S)-3-methyl-1-(pyridin-2-yl)butan-1-amine(144852-40-4)
• EPA Substance Registry System: (S)-3-methyl-1-(pyridin-2-yl)butan-1-amine(144852-40-4)

Safety Data

• Hazardous Substances Data: 144852-40-4(Hazardous Substances Data)

Upstream product

• 825647-69-6 3-methyl-1-(pyridin-2-yl)butan-1-amine 
• 2419-38-7 N-phthaloyl-(S)-leucine 
• 144902-13-6 (S)-4-methyl-2-(phthaloylamino)pentanenitrile 
• 38509-54-5 (S)-2-(1,3-dioxoisoindolin-2-yl)-4-methylpentanamide 
• 144852-22-2 (S)-3-methyl-N-phthaloyl-1-(2-pyridyl)butylamine 

Relevant articles and documents

KINASE INHIBITORS AND METHOD OF TREATING CANCER WITH SAME

The present teachings provide a compound represented by structural formula (I): or a pharmaceutically acceptable salt thereof. Also described are pharmaceutical compositions and methods of use thereof.

KINASE INHIBITORS AND METHOD OF TREATING CANCER WITH SAME

The invention is a compound represented by Structural Formula (I) or a pharmaceutically acceptable salt thereof. Values for the variables are provided herein. Also included is a pharmaceutical composition comprising the compound represented by Structural Formula (I) and a pharmaceutically acceptable carrier or diluent and methods of treating a subject with cancer with the compound of Structural Formula (I).

INDAZOLE COMPOUNDS AS KINASE INHIBITORS AND METHOD OF TREATING CANCER WITH SAME

The present teaching provide indazole compounds represented by Structural Formulae (I) or (I') or a pharmaceutically acceptable salt thereof. Also described are pharmaceutical compositions and methods of use thereof as protein kinase inhibitors, such as T

Chiral ligands containing heteroatoms; 9. General procedures for the synthesis of optically active 1-(2-pyridyl)alkylamines from α-amino acids

General syntheses of 1-(2-pyridyl)alkylamines and N-methyl or N,N-dimethyl-1-(2-pyridyl)alkylamines from optically active α-amino acids are described. The presented procedures are based on catalyzed co-cyclotrimerization of the suitable nitriles with acet