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2-chloro-1,3,3-triphenylprop-2-en-1-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

38185-94-3

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38185-94-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 38185-94-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,8,1,8 and 5 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 38185-94:
(7*3)+(6*8)+(5*1)+(4*8)+(3*5)+(2*9)+(1*4)=143
143 % 10 = 3
So 38185-94-3 is a valid CAS Registry Number.

38185-94-3Downstream Products

38185-94-3Relevant academic research and scientific papers

Preparation of Triazole Gold(III) Complex as an Effective Catalyst for the Synthesis of E-α-Haloenones

Yang, Yongchun,Hu, Wenkang,Ye, Xiaohan,Wang, Dawei,Shi, Xiaodong

, p. 2583 - 2588 (2016)

The pyridyltriazole ligand was prepared and applied as a new ligand system for the coordination towards gold(III) cations. The resulting complex showed excellent stability and effective catalytic reactivity for the Meyer–Schuster rearrangement of propargyl alcohols and sequential allene halogenation, giving α-haloenones with excellent yields and good E/Z selectivity. More importantly, by using this new gold(III) catalytic system, the challenging α-chloroenone substrates were synthesized in good yields for the first time. This work also permits the avoidance of preparing of acetate derivatives as required in the case of Au(I) catalysts and validates that the triazole gold(III) complex is an effective new catalyst for alkyne activation. (Figure presented.).

"Wolf and lamb" reactions: Equilibrium and kinetic effects in multipolymer systems

Cohen,Kraus,Patchornik

, p. 7620 - 7629 (2007/10/02)

Two reagents reacting avidly with each other in solution are rendered mutually inactive by attaching each to a separate batch of insoluble polymer. Two-stage reactions in which a soluble reagent reacts first with one polymeric reagent and the product with the second polymeric reagent afford advantages over analogous reactions in solution. In acylation reactions of carbon acids, the simultaneous use of a polymeric strong base and a polymeric acylating reagent proved to be superior to the use of soluble reagents, both for bringing about quantitative acylations and for coping with undesirable side reactions. New polymeric strong bases were prepared: polymeric trityllithium, para-substituted trityllithium polymers, and polymeric lithium diisopropylamide. Active esters of polymeric o-nitrophenol and N-1-hydroxybenzotriazole were used as acylation reagents. The scope and limitation of these reactions and their application to general multiphase systems are discussed.

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