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Benzene, 1-(1,3-butadienyl)-2-methyl-, (Z)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

34599-76-3

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34599-76-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 34599-76-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,4,5,9 and 9 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 34599-76:
(7*3)+(6*4)+(5*5)+(4*9)+(3*9)+(2*7)+(1*6)=153
153 % 10 = 3
So 34599-76-3 is a valid CAS Registry Number.

34599-76-3Downstream Products

34599-76-3Relevant academic research and scientific papers

Selective 1,2-Aminoisothiocyanation of 1,3-Dienes Under Visible-Light Photoredox Catalysis

Guo, Weisi,Wang, Qian,Zhu, Jieping

, p. 4085 - 4089 (2021)

Selective three-component 1,2-diamination of 1,3-dienes with concurrent introduction of two orthogonally protected amino groups remains unknown despite its significant synthetic potential. We report herein that reaction of conjugated dienes with N-aminopy

Photoinduced Palladium-Catalyzed Carbofunctionalization of Conjugated Dienes Proceeding via Radical-Polar Crossover Scenario: 1,2-Aminoalkylation and beyond

Gevorgyan, Vladimir,Kurandina, Daria,Shing Cheung, Kelvin Pak,Yata, Tetsuji

supporting information, p. 9932 - 9937 (2020/06/27)

A photoinduced palladium-catalyzed 1,2-carbofunctionalization of conjugated dienes has been developed. This mild modular approach, which does not require employment of exogeneous photosensitizers and external oxidants, allows for efficient and highly regio- and stereoselective synthesis of a broad range of allylic amines from readily available 1,3-dienes, alkyl iodides, and amines. Employment of O- and C-nucleophiles toward oxyalkylation and dialkylation products was also demonstrated. A putative π-allyl palladium radical-polar crossover path is proposed as a key event in this three-component coupling process. The utility of this protocol is highlighted by its application for derivatization of several amine-containing drugs.

Cu-Catalyzed highly regioselective 1,2-hydrocarboxylation of 1,3-dienes with CO2

Zhang, Penglin,Zhou, Zhanglang,Zhang, Rumeng,Zhao, Qian,Zhang, Chun

supporting information, p. 11469 - 11472 (2020/10/12)

A practical copper-catalyzed highly regioselective 1,2-hydrocarboxylation of terminal 1,3-diene with carbon dioxide has been developed. Under mild reaction conditions, this chemistry afforded 2-benzyl-β,γ-unsaturated acid derivatives as products, which are a kind of important unit for bio-active molecules and versatile precursors for organic synthesis, with good functional group tolerance. The key intermediate in this transformation is illustrated by control experiments.

Ni-Catalyzed Site-Selective Dicarboxylation of 1,3-Dienes with CO2

Tortajada, Andreu,Ninokata, Ryo,Martin, Ruben

supporting information, p. 2050 - 2053 (2018/02/19)

A site-selective catalytic incorporation of multiple CO2 molecules into 1,3-dienes en route to adipic acids is described. This protocol is characterized by its mild conditions, excellent chemo- and regioselectivity and ease of execution under CO2 (1 atm), including the use of bulk butadiene and/or isoprene feedstocks.

Catalyst Controlled Regiodivergent Arylboration of Dienes

Sardini, Stephen R.,Brown, M. Kevin

supporting information, p. 9823 - 9826 (2017/08/02)

A method for the regiodivergent arylboration of dienes is presented. These reactions allow for the formation of a diverse range of synthetically versatile products from simple precursors. Through mechanistic studies, these reactions likely operate by init

Superoxide mediated isomerization of 4-aryl-but-1-ynes to 1-aryl-1,3-butadienes

Khan, Faiz Ahmed,Budanur, Basavaraj M.

, p. 7600 - 7607 (2015/09/07)

A new role of superoxide ion in the isomerization of homobenzylic acetylenes leading to 1-aryl-1,3-butadienes is reported. The unconventional reagent KO2 is found to be superior in performing this kind of isomerization over other the commonly u

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