482620-71-3 Usage
Description
Methanone, [4-[(1S)-1-aminoethyl]phenyl]phenylis a complex chemical compound that features a methanone group (C=O) connected to a phenyl ring, which is substituted with a 1-aminoethyl group. Methanone, [4-[(1S)-1-aminoethyl]phenyl]phenylis of interest in the fields of medicinal chemistry and pharmaceutical research due to its intricate molecular structure and potential therapeutic properties.
Uses
Used in Pharmaceutical Research:
Methanone, [4-[(1S)-1-aminoethyl]phenyl]phenylis utilized as a research compound for exploring its potential therapeutic applications. Its unique structure and pharmacological activity make it a promising candidate for the development of new drugs to treat various medical conditions.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, Methanone, [4-[(1S)-1-aminoethyl]phenyl]phenylserves as a subject of interest for scientists and researchers. Its complex structure and potential interactions with biological targets are being investigated to understand its full range of uses and effects, which may lead to advancements in drug discovery and design.
Check Digit Verification of cas no
The CAS Registry Mumber 482620-71-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,8,2,6,2 and 0 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 482620-71:
(8*4)+(7*8)+(6*2)+(5*6)+(4*2)+(3*0)+(2*7)+(1*1)=153
153 % 10 = 3
So 482620-71-3 is a valid CAS Registry Number.
InChI:InChI=1/C15H15NO/c1-11(16)12-7-9-14(10-8-12)15(17)13-5-3-2-4-6-13/h2-11H,16H2,1H3/t11-/m0/s1
482620-71-3Relevant articles and documents
Studies on the enantioselective catalysis of photochemically promoted transformations: "Sensitizing receptors" as chiral catalysts
Cauble, David F.,Lynch, Vincent,Krische, Michael J.
, p. 15 - 21 (2007/10/03)
A strategy for the enantioselective catalysis of photomediated reactions in solution is described, involving the use of chiral molecular receptors possessing appendant triplet-sensitizing moieties. Energy transfer is selectively directed to bound substrate as a consequence of the distance dependence of triplet-triplet energy transfer. This effect, which is equivalent to a binding-induced rate enhancement, enables substoichiometric chirality transfer from the receptor template to the substrate, as observed in the intramolecular enone-olefin photo [2 + 2]cycloaddition of a quinolone substrate.
