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(R)-1-(4-chlorophenyl)allyl acetate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1362084-89-6

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1362084-89-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1362084-89-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,6,2,0,8 and 4 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1362084-89:
(9*1)+(8*3)+(7*6)+(6*2)+(5*0)+(4*8)+(3*4)+(2*8)+(1*9)=156
156 % 10 = 6
So 1362084-89-6 is a valid CAS Registry Number.

1362084-89-6Downstream Products

1362084-89-6Relevant academic research and scientific papers

Base-Free Dynamic Kinetic Resolution of Secondary Alcohols with a Ruthenium-Lipase Couple

Yun, Inyeol,Park, Jin Yong,Park, Jaiwook,Kim, Mahn-Joo

, p. 16293 - 16298 (2019/12/27)

We report the dynamic kinetic resolution (DKR) of various secondary alcohols by the combination of a ruthenium catalyst and an anionic surfactant-activated lipoprotein lipase. The DKR reactions performed under totally base-free conditions at room temperature provided the products of excellent enantiopurities (91-99% ee or greater) in high yields (92-99%). More importantly, the DKR of α-arylallyl alcohols was achieved for the first time with high yields (87-91%).

Highly efficient kinetic resolution of allylic alcohols with terminal double bond

Marques, Francisco A.,Oliveira, Marcos A.,Frensch, Gustavo,Sales Maia, Beatriz Helena L. N.,Barison, Andersson,Lenz, Cesar A.,Guerrero Jr., Palimecio G.

, p. 696 - 700 (2012/06/04)

In this study, the lipase-catalyzed kinetic resolution (Novozyme 435) was employed to prepare chiral allylic alcohols and acetates with terminal double bonds in enantiomeric excesses ranging from 94 to >99 %.

A new mathematical method for determining the enantiomeric ratio in lipase-catalyzed reactions

Mitchell, David Alexander,Moure, Vivian Rotuno,Marques, Francisco de Assis,Krieger, Nadia

experimental part, p. 23 - 28 (2010/11/02)

We present a new mathematical method for determining the enantiomeric ratio (E) during lipase-catalyzed kinetic resolutions. The method involves the fitting of a model to profiles of adimensionalized concentrations of the two enantiomers of the chiral substrate, plotted against degree of conversion. The model equations are presented for a reversible reaction involving bi-bi ping-pong kinetics in which the chiral substrate enters second and the chiral product leaves second. However, it is also shown that the method is easy to modify for analysis of resolutions involving other chiral substrate-product pairs and of resolutions in which the behavior of the system can be approximated by irreversible uni-uni kinetics. We show that our method retains several advantageous features of existing methods that help to ensure accuracy.

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