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3-benzylchroman-4-ol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

417710-59-9

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417710-59-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 417710-59-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,1,7,7,1 and 0 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 417710-59:
(8*4)+(7*1)+(6*7)+(5*7)+(4*1)+(3*0)+(2*5)+(1*9)=139
139 % 10 = 9
So 417710-59-9 is a valid CAS Registry Number.

417710-59-9Downstream Products

417710-59-9Relevant academic research and scientific papers

Rhodium-Catalyzed Asymmetric Transfer Hydrogenation/Dynamic Kinetic Resolution of 3-Benzylidene-Chromanones

Molina Betancourt, Ricardo,Phansavath, Phannarath,Ratovelomanana-Vidal, Virginie

, p. 1621 - 1625 (2021)

Straightforward access to enantiomerically enriched cis-3-benzyl-chromanols from (E)-3-benzylidene-chromanones was developed through Rh-catalyzed asymmetric transfer hydrogenation. This transformation allowed the reduction of both the CaC and CaO bonds and the formation of two stereocenters in high yields with excellent levels of diastereo- A nd enantioselectivities (up to >99:1 dr, up to >99% ee) in a single step through a dynamic kinetic resolution process using a low catalyst loading and HCO2H/DABCO as the hydrogen source.

Photoredox-Catalyzed Ketyl-Olefin Coupling for the Synthesis of Substituted Chromanols

Fava, Eleonora,Nakajima, Masaki,Nguyen, Anh L. P.,Rueping, Magnus

supporting information, p. 6959 - 6964 (2016/08/30)

A visible light photoredox-catalyzed aldehyde olefin cyclization is reported. The method represents a formal hydroacylation of alkenes and alkynes and provides chromanol derivatives in good yields. The protocol takes advantage of the double role played by trialkylamines (NR3) which act as (i) electron donors for reducing the catalyst and (ii) proton donors to activate the substrate via a proton-coupled electron transfer.

Urea derivatives useful as anticancer agents

-

, (2008/06/13)

The present invention relates to compounds of formula I And to pharmaceutically acceptable salts, hydrates and prodrugs thereof, wherein R1, R2, R3, R4, R5, R10, R11, b, m, n, p and v are as defined herein. The invention also relates to pharmaceutical compositions containing the above compounds and methods of treating hyperproliferative disorders in mammals by administering the above compounds.

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