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(R)-1-(3-chloroethylphenyl)ethyl acetate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

136705-69-6

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136705-69-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 136705-69-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,6,7,0 and 5 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 136705-69:
(8*1)+(7*3)+(6*6)+(5*7)+(4*0)+(3*5)+(2*6)+(1*9)=136
136 % 10 = 6
So 136705-69-6 is a valid CAS Registry Number.

136705-69-6Downstream Products

136705-69-6Relevant academic research and scientific papers

CO2-expanded liquids as solvents to enhance activity of Pseudozyma antarctica lipase B towards ortho-substituted 1-phenylethanols

Hoang, Hai Nam,Koesoema, Afifa Ayu,Matsuda, Tomoko,Otsu, Moeko,Suzuki, Yuichi,Tamura, Mayumi

supporting information, (2020/09/18)

Pseudozyma (Candida) antarctica lipase B (CAL-B, Novozym 435) is one of the most widely used and outstanding biocatalysts. However, CAL-B-catalyzed transesterification of ortho-substituted 1-phenylethanol analogs suffers low conversion. In this research, the reactions were accelerated by using CO2-expanded liquids, liquids expanded by dissolving pressurized CO2, such as CO2-expanded hexane or CO2-expanded MeTHF.

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%).

Stereochemistry and mechanism of enzymatic and non-enzymatic hydrolysis of benzylic sec-sulfate esters

Toesch, Michael,Schober, Markus,Breinbauer, Rolf,Faber, Kurt

supporting information, p. 3930 - 3934 (2014/06/24)

The substrate scope of inverting alkylsulfatase Pisa1 was extended towards benzylic sec-sulfate esters by suppression of competing non-enzymatic autohydrolysis by addition of dimethyl sulfoxide as co-solvent. Detailed investigation of the mechanism of autohydrolysis in 18O-labeled buffer by using an enantiopure sec-benzylic sulfate ester as substrate revealed that from the three possible pathways (i) inverting SN2-type nucleophilic attack of [OH-] at the benzylic carbon represents the major pathway, whereas (ii) SN1-type formation of a planar benzylic carbenium ion leading to racemization was a minor event, and (iii) Retaining SN2-type nucleophilic attack at sulfur took place at the limits of detection. The data obtained are interpreted by analysis of Hammett constants of meta substituents. The enzymatic hydrolysis of benzylic sec-sulfate esters by alkylsulfatase Pisa1 proceeded with clean inversion of configuration and with excellent stereoselectivities when the competing non-enzymatic hydrolysis was suppressed by addition of dimethyl sulfoxide as co-solvent. Copyright

A Cationic Ruthenium Complex for the Dynamic Kinetic Resolution of Secondary Alcohols

Fernández-Salas, José A.,Manzini, Simone,Nolan, Steven P.

supporting information, p. 13132 - 13135 (2016/02/19)

A synthetic protocol making use of a well-defined cationic ruthenium complex 2 enabling the racemization of enantiomerically pure secondary alcohols in the presence of a weak base (K2CO3) is described. The compatibility of 2 with Candida Antarctica lipase B (Novozym 435) allows the development of an efficient dynamic kinetic resolution of sec-alcohols in the absence of an additional strong base. This procedure involves the first example of a dynamic kinetic resolution of alcohols in the presence of a cationic ruthenium catalyst. In addition, we describe the conversion of ketones to the enantioenriched acetates in a one-pot reaction, probing the versatility of complex 2.

Highly efficient dynamic kinetic resolution of secondary aromatic alcohols with low-cost and easily available acid resins as racemization catalysts

Cheng, Yongmei,Xu, Gang,Wu, Jianping,Zhang, Chensheng,Yang, Lirong

experimental part, p. 2366 - 2369 (2010/06/13)

A new and efficient dynamic kinetic resolution (DKR) process of secondary aromatic alcohols was developed with acid resins as racemization catalysts. Acid resin CD8604 was shown to have excellent racemization activity and good biocompatibility. When employing CD8604 and complex acyl donors as racemization catalyst and acyl donor, respectively, enantiomerically pure aromatic acetate was obtained with excellent yield and ee values through the DKR process. It is noteworthy that the system could be reused more than 10 times with little loss of yield and ee value.

Immobilized Manihot esculenta preparation as a novel biocatalyst in the enantioselective acetylation of racemic alcohols

Machado, Luciana L.,Lemos, Telma L.G.,de Mattos, Marcos Carlos,de Oliveira, Maria da Conceicao F.,de Gonzalo, Gonzalo,Gotor-Fernandez, Vicente,Gotor, Vicente

, p. 1418 - 1423 (2008/12/20)

The enzymatic preparation obtained from a discard of Manihot esculenta roots has been successfully immobilized on calcium alginate hydrogels. This preparation has been tested as a chiral biocatalyst in the enzymatic acylation of a set of racemic aromatic alcohols. Depending on the reaction conditions, excellent enantioselectivities can be achieved. Some parameters that can alter the biocatalytic properties of the enzyme, such as solvent, temperature, acyl donor and substrate structure have been studied exhaustively in order to establish a deeper knowledge of this novel biocatalyst.

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