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Benzamide, N-(4-ethenylphenyl)-, also known as 4-vinylaniline benzamide, is an organic compound with the chemical formula C15H13NO. It is a derivative of benzamide, where a 4-ethenylphenyl group is attached to the nitrogen atom. Benzamide, N-(4-ethenylphenyl)- is characterized by its aromatic structure, with a benzene ring and a vinyl group attached to the nitrogen atom of the amide functional group. It is used in various chemical and pharmaceutical applications, such as the synthesis of dyes, pharmaceuticals, and other organic compounds. Due to its reactivity and potential applications, it is an important compound in the field of organic chemistry.

7297-64-5

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7297-64-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7297-64-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,2,9 and 7 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 7297-64:
(6*7)+(5*2)+(4*9)+(3*7)+(2*6)+(1*4)=125
125 % 10 = 5
So 7297-64-5 is a valid CAS Registry Number.

7297-64-5Downstream Products

7297-64-5Relevant academic research and scientific papers

Chiroptical properties of graft copolymers containing chiral poly(n -hexyl isocyanate) as a side chain

Shah, Priyank N.,Min, Joonkeun,Kim, Hyung-Jin,Park, Sang-Yoon,Lee, Jae-Suk

, p. 7917 - 7925 (2011)

Chiral poly(n-hexyl isocyanate) (PHIC) macromonomers were synthesized by living anionic polymerization of n-hexyl isocyanate (HIC) using the functional initiator sodium N-(4-vinylphenyl)benzamide (Na-4VPBA) in tetrahydrofuran (THF) at -98 °C. Polymerizati

Visible-Light-Promoted Iron-Catalyzed N-Arylation of Dioxazolones with Arylboronic Acids

Tang, Jing-Jing,Yu, Xiaoqiang,Yamamoto, Yoshinori,Bao, Ming

, p. 13955 - 13961 (2021/11/20)

A visible-light-promoted and simple iron salt-catalyzed N-arylation was achieved efficiently under external photosensitizer-free conditions. Arylboronic acids and bench-stable dioxazolones were used for this cross-coupling reaction. This reaction features high reactivity, wide substrate scope, good functional group tolerance, simple operation procedure, and mild reaction conditions. Preliminary mechanistic investigations were conducted to support a radical pathway. This method may contribute to shift the paradigm of iron-catalyzed C-N bond construction and nitrene transfer chemistry.

Synthesis of 2-Amino-1,3-dienes from Propargyl Carbonates via Palladium-Catalyzed Carbon-Nitrogen Bond Formation

O'Broin, Calvin Q.,Guiry, Patrick J.

supporting information, p. 879 - 883 (2020/02/04)

A catalytic method to synthesize 1,3,-dienes from propargylic precursors is reported. This palladium-catalyzed carbon-nitrogen bond-forming reaction furnishes 2-amino-1,3-dienes in excellent yields (up to 98%) and shows a broad tolerance to functional group diversity. The reaction has been demonstrated for over 30 amine substrates, including anilines and indoles, and proceeds under mild neutral conditions. The resulting 1,3-dienes are of great synthetic interest because of their further reaction potential.

An easy access to styrenes: Trans aryl 1,3-, 1,4- and 1,5-dienes, and 1,3,5-trienes by Hiyama cross-coupling catalyzed by palladium nanoparticles

Chatterjee, Tanmay,Dey, Raju,Ranu, Brindaban C.

experimental part, p. 1103 - 1110 (2011/07/08)

A convenient and efficient procedure has been developed for the vinylation of aryl-, styrenyl-, cinnamyl- and dienyl-halides by a Pd(0) nanoparticle-catalyzed Hiyama cross-coupling to provide the corresponding dienes and trienes in high yields. The reaction does not require any ligand or co-catalyst, and is carried out using PdCl2 and tetrabutyl ammonium fluoride (TBAF) in THF. Pd nanoparticles are generated in situ and are the active catalytic species in this reaction. A wide range of functionalized styrenes, trans aryl 1,3-, 1,4- and 1,5- dienes, 1,2-, 1-3 and 1,4-bis(1,3-dienes), and 1,3,5-trienes can be obtained by this procedure. The Royal Society of Chemistry and the Centre National de la Recherche Scientifique 2011.

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