59108-53-1 Usage
Uses
Used in Pharmaceutical Industry:
CHROMAN-3-YLAMINE is used as a building block in organic synthesis for the development of new pharmaceuticals. Its unique structure and properties make it a valuable component in the creation of various drug molecules.
Used in Agrochemical Industry:
CHROMAN-3-YLAMINE is used as a precursor in the synthesis of agrochemicals, contributing to the development of effective and environmentally friendly pesticides and other agricultural products.
Used in Anti-inflammatory Applications:
CHROMAN-3-YLAMINE is used as an anti-inflammatory agent due to its potential to modulate inflammatory pathways and reduce inflammation in various conditions.
Used in Antioxidant Applications:
CHROMAN-3-YLAMINE is used as an antioxidant agent, helping to neutralize free radicals and protect cells from oxidative damage, which can contribute to various diseases and aging processes.
Used in Neurodegenerative Disease Treatment:
CHROMAN-3-YLAMINE is used in the research and development of treatments for neurodegenerative diseases such as Parkinson's and Alzheimer's, due to its potential neuroprotective properties and ability to target specific pathways involved in these conditions.
Check Digit Verification of cas no
The CAS Registry Mumber 59108-53-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,9,1,0 and 8 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 59108-53:
(7*5)+(6*9)+(5*1)+(4*0)+(3*8)+(2*5)+(1*3)=131
131 % 10 = 1
So 59108-53-1 is a valid CAS Registry Number.
InChI:InChI=1/C9H11NO/c10-8-5-7-3-1-2-4-9(7)11-6-8/h1-4,8H,5-6,10H2/t8-/m1/s1
59108-53-1Relevant academic research and scientific papers
Pressnitz, Desiree,Fuchs, Christine S.,Sattler, Johann H.,Knaus, Tanja,Macheroux, Peter,Mutti, Francesco G.,Kroutil, Wolfgang
, p. 555 - 559 (2013)
Various (S)-selective and (R)-selective ω-transaminases were investigated for the amination of 1- and 2-tetralone and derivatives as well as of 3- and 4-chromanone. All ketones tested were aminated to give the corresponding enantiopure amines (ee > 99%) employing at least one of the enzymes investigated. In most of the cases the (S)- as well as the (R)-enantiomer was obtained in optically pure form. The amination of 3-chromanone was performed on a 100 mg scale leading to optically pure (R)-3-aminochromane (ee > 99%) with complete conversion and 78% isolated yield.
