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Bis(2-phenylethynyl)zinc is an organozinc compound with the chemical formula Zn(C≡CPh)2, where "Ph" represents a phenyl group. It is a colorless, crystalline solid that is sensitive to air and moisture. bis(2-phenylethynyl)zinc is primarily used as a reagent in organic synthesis, particularly in cross-coupling reactions, such as the Sonogashira coupling, which involves the formation of carbon-carbon bonds between terminal alkynes and aryl or vinyl halides. Bis(2-phenylethynyl)zinc is synthesized by the reaction of zinc metal with 2-phenylethynyllithium or 2-phenylethynylmagnesium bromide. Due to its reactivity, it is typically handled under an inert atmosphere, such as nitrogen or argon, to prevent unwanted side reactions.

1085-51-4

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1085-51-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1085-51-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,8 and 5 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1085-51:
(6*1)+(5*0)+(4*8)+(3*5)+(2*5)+(1*1)=64
64 % 10 = 4
So 1085-51-4 is a valid CAS Registry Number.

1085-51-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name bis(2-phenylethynyl)zinc

1.2 Other means of identification

Product number -
Other names .Bis-<phenethinyl>-zink

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:1085-51-4 SDS

1085-51-4Relevant academic research and scientific papers

Et2Zn-mediated stoichiometric C(sp)-H silylation of 1-alkynes and chlorosilanes

Huang, Pan,Xu, Dawen,Reich, Robert M.,Kaiser, Felix,Liu, Boping,Kühn, Fritz E.

, p. 1574 - 1577 (2019)

A first example of an Et2Zn mediated silylation of 1-aklynes is reported. A series of functional groups are tolerated in this reaction. Mechanistic studies support Zn alkynilides as intermediates in the reaction. This reaction protocol provides a practical method for the preparation of alkynylsilanes and expands the application of organometallic zinc in organic synthesis.

Three-Component Difunctionalization of Cyclohexenyl Triflates: Direct Access to Versatile Cyclohexenes via Cyclohexynes

Cho, Seoyoung,McLaren, E. J.,Wang, Qiu

supporting information, p. 26332 - 26336 (2021/11/10)

Difunctionalization of strained cyclic alkynes presents a powerful strategy to build richly functionalized cyclic alkenes in an expedient fashion. Herein we disclose an efficient and flexible approach to achieve carbohalogenation, dicarbofunctionalization, aminohalogenation and aminocarbonation of readily available cyclohexenyl triflates. We have demonstrated the novel use of zincate base/nucleophile system for effective formation of key cyclohexyne intermediates and selective addition of various carbon and nitrogen nucleophiles. Importantly, leveraging the resulting organozincates enables the incorporation of a broad range of electrophilic partners to deliver structurally diverse cyclohexene motifs. The importance and utility of this method is also exemplified by the modularity of this approach and the ease in which even highly complex polycyclic scaffolds can be accessed in one step.

Alkylation of Terminal Alkynes under Zinc Lewis Acid Catalysis and Its Mechanistic Studies

Osano, Mana,Kida, Takeru,Yonekura, Kyohei,Tsuchimoto, Teruhisa

supporting information, p. 2825 - 2831 (2019/04/13)

With a zinc Lewis acid catalyst and proton sponge in toluene, terminal alkynes were found to undergo the alkylation by alkyl triflates to provide unsymmetrical internal alkynes. This is the first example that a simple alkyl chain other than benzylic and norbornyl units can be introduced onto the alkynyl carbon atom under Lewis acid catalysis. Mechanistic studies revealed that the activation of the alkyne by the zinc Lewis acid and proton sponge is the trigger of the reaction to give a monoalkynylzinc species, which successively reacts with the alkyl triflate to afford the internal alkyne. A radical pathway is unlikely in this system. (Figure presented.).

Decarboxylative Negishi Coupling of Redox-Active Aliphatic Esters by Cobalt Catalysis

Liu, Xu-Ge,Zhou, Chu-Jun,Lin,Han, Xiang-Lei,Zhang, Shang-Shi,Li, Qingjiang,Wang, Honggen

supporting information, p. 13096 - 13100 (2018/09/21)

A cobalt-catalyzed decarboxylative Negishi coupling reaction of redox-active aliphatic esters with organozinc reagents was developed. The method enabled efficient alkyl–aryl, alkyl–alkenyl, and alkyl–alkynyl coupling reactions under mild reaction conditions with no external ligand or additive needed. The success of an in situ activation protocol and the facile synthesis of the drug molecule (±)-preclamol highlight the synthetic potential of this method. Mechanistic studies indicated that a radical mechanism is involved.

Single electron transfer-induced coupling of alkynylzinc reagents with aryl and alkenyl iodides

Okura, Keisho,Kawashima, Hitomi,Tamakuni, Fumiko,Nishida, Naoya,Shirakawa, Eiji

supporting information, p. 14019 - 14022 (2016/12/09)

Alkynylzinc reagents were found to undergo coupling with aryl and alkenyl iodides to give arylalkynes and alkenylalkynes without the aid of transition metals. The coupling reaction proceeds through a single electron transfer mechanism, where a substoichiometric amount of a phosphine works as an indispensable activator.

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