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3-(4-methylphenyl)- and 3-(4-methoxyphenyl)propargyl chloride is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

16017-25-7

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16017-25-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 16017-25-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,0,1 and 7 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 16017-25:
(7*1)+(6*6)+(5*0)+(4*1)+(3*7)+(2*2)+(1*5)=77
77 % 10 = 7
So 16017-25-7 is a valid CAS Registry Number.

16017-25-7Upstream product

16017-25-7Relevant academic research and scientific papers

Copper(I)-catalyzed regioselective propargylic substitution involving Si-B bond activation

Vyas, Devendra J.,Hazra, Chinmoy K.,Oestreich, Martin

, p. 4462 - 4465 (2011)

The silicon nucleophile generated by copper(I)-catalyzed Si-B bond activation allows several γ-selective propargylic substitutions. The regioselectivity (γ:α ratio) is strongly dependent on the propargylic leaving group. Chloride is superior to oxygen leaving groups in linear substrates (γ:α > 99:1), and it is only the phosphate group that also shows promising regiocontrol (γ:α = 90:10). That leaving group produces superb γ-selectivity (γ:α > 99:1) in α-branched propargylic systems, and enantioenriched substrates react with excellent central-to-axial chirality transfer.

Copper-catalyzed nucleophilic trifluoromethylation of propargylic halides

Miyake, Yoshihiro,Ota, Shin-Ichi,Shibata, Masashi,Nakajima, Kazunari,Nishibayashi, Yoshiaki

supporting information, p. 7809 - 7811 (2013/09/02)

Reactions of propargylic halides with trifluoromethyltrimethylsilane in the presence of a catalytic amount of copper(i) thiophene-2-carboxylate (CuTC) have been found to give the corresponding trifluoromethylated products in good to high yields with a hig

Copper(I)-catalyzed regio- and chemoselective single and double addition of nucleophilic silicon to propargylic chlorides and phosphates

Hazra, Chinmoy K.,Oestreich, Martin

supporting information; experimental part, p. 4010 - 4013 (2012/10/08)

Copper(I)-catalyzed propargylic substitution of linear precursors with (Me2PhSi)2Zn predominantly yields the γ isomer independent of the propargylic leaving group. The thus formed allenylic silane reacts regioselectively with another equivalent of (Me2PhSi) 2Zn, yielding a bifunctional building block with allylic and vinylic silicon groups. The reaction rates of both steps are well-balanced for chloride (γ:α ≥ 99:1) where the propargylic displacement occurs quantitatively prior to the addition step. Substitutions of α-branched propargylic phosphates are also reported.

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