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1-(3,5-bis(tri-fluoromethyl)phenyl)-3-(pyridin-2-yl)thiourea is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1154050-98-2

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1154050-98-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1154050-98-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,5,4,0,5 and 0 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1154050-98:
(9*1)+(8*1)+(7*5)+(6*4)+(5*0)+(4*5)+(3*0)+(2*9)+(1*8)=122
122 % 10 = 2
So 1154050-98-2 is a valid CAS Registry Number.

1154050-98-2Downstream Products

1154050-98-2Relevant academic research and scientific papers

Dynamic assembly of a zinc-templated bifunctional organocatalyst in the presence of water for the asymmetric aldol reaction

Serra-Pont, Anna,Alfonso, Ignacio,Jimeno, Ciril,Solà, Jordi

, p. 17386 - 17389 (2015)

A bifunctional organocatalytic system consisting of simple pyridine ligands containing separate catalytic functionalities was assembled using ZnCl2. This novel metal-templated catalyst furnished high yields and stereoselectivities towards the a

Synergetic Organocatalysis for Eliminating Epimerization in Ring-Opening Polymerizations Enables Synthesis of Stereoregular Isotactic Polyester

Tao, Youhua,Li, Maosheng,Tao, Yue,Tang, Jiadong,Wang, Yanchao,Zhang, Xiaoyong,Wang, Xianhong

supporting information, p. 281 - 289 (2019/01/04)

Ring-opening polymerization of O-carboxyanhydrides (OCAs) can furnish polyesters with a diversity of functional groups that are traditionally hard to harvest by polymerization of lactones. Typical ring-opening catalysts are subject to unavoidable racemization of most OCA monomers, which hampers the synthesis of highly isotactic crystalline polymers. Here, we describe an effective bifunctional single-molecule organocatalysis for selective ring-opening polymerization of OCAs without epimerization. The close vicinity of both activating groups in the same molecule engenders an amplified synergetic effect and thus allows for the use of mild bases, thereby leading to minimal epimerization for polymerization. Ring-opening polymerization of manOCA monomer (OCA from mandelic acid) mediated by the bifunctional single-molecule organocatalyst yields highly isotactic poly(mandelic acid) (PMA) with controlled molecular weights (up to 19.8 kg mol-1). Mixing of the two enantiomers of PMA generates the first example of a crystalline stereocomplex in this area, which displayed distinct Tm values around 150 °C. Remarkably, the bifunctional catalysts are moisture-stable, recyclable, and easy to use, allowing sustainable and scalable synthesis of a stereoregular functional polyester.

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