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4-[2-(pyridin-4-yl)ethenyl]phenyl acetate is an organic compound with the molecular formula C15H13NO2. It is a derivative of phenyl acetate, featuring a pyridine ring attached to the phenyl group through an ethene bridge. This chemical is characterized by its aromatic structure, with the pyridine ring contributing to its nitrogen-containing heteroaromatic nature. It is likely to be used in the synthesis of more complex molecules, potentially in pharmaceuticals or materials science, due to its unique structural features. The compound's properties, such as solubility and reactivity, would be influenced by the presence of the pyridine ring and the ester group, making it a versatile building block for further chemical modifications.

2298-21-7

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2298-21-7 Usage

Type of compound

Acetate ester derivative

Structure

Substituted phenyl compound with a pyridine ring attached to the ethenyl group

Uses

Pharmaceutical research, drug development, synthesis of organic compounds

Properties

Potential ligand in metal complexation and catalysis, potential biological activity in drug discovery

Future potential

Further studies and research may reveal additional applications in various fields

Check Digit Verification of cas no

The CAS Registry Mumber 2298-21-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,2,9 and 8 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 2298-21:
(6*2)+(5*2)+(4*9)+(3*8)+(2*2)+(1*1)=87
87 % 10 = 7
So 2298-21-7 is a valid CAS Registry Number.

2298-21-7Relevant academic research and scientific papers

Use of intermolecular hydrogen bonding for the induction of liquid crystallinity in the side chain of polysiloxanes

Kumar, Uday,Kato, Takashi,Fréchet, Jean M. J.

, p. 6630 - 6639 (2007/10/02)

A new type of liquid crystalline side chain polysiloxane has been built through self-assembly via intermolecular hydrogen bonding between H-bond donor and acceptor moieties. Poly(methylsiloxanes) and poly(methyl-co-dimethylsiloxanes) with side chains cont

MICROENVIRONMENT OF POLYMER CHAINS IN SOLUTION: pKa OF INDICATORS BOUND TO THE POLYMER CHAIN

Mikes, Frantisek,Labsky, Jiri,Vyprachticky, Drahomir,Chalabala, Jiri

, p. 2226 - 2232 (2007/10/02)

Polymers bearing at the end of side chains acidobasic indicator moieties exhibiting a solvatochromic absorption band were prepared by a polymeranalogous reaction of copolymers N-(2-hydroxy propyl) methacrylamide-N-methacryloylated 4-nitrophenyl ester ω-am

Kinetics of Reaction of Phenacyl Bromide with 3- and 4-Substituted Pyridines and 4-Substituted 4-Styrylpyridines

Shunmugasundaram, A.,Balakumar, S.

, p. 775 - 777 (2007/10/02)

The rates of reaction of phenacyl bromide with 3- and 4-substituted pyridines and 4'-substituted 4-styrylpyridines have been measured in aq. acetone (90percent, v/v) at 30 deg C, 35 deg C and 40 deg C and the activation parameters have been evaluated.Satisfactory Hammett correlations are obtained for both pyridine and styrylpyridine series.The effectiveness of transmission of substituent effect in styrylpyridine system relative to pyridine system in this reaction is calculated to be 0.104.From the Bronsted relationship the coefficient (βN) is found to be 0.48, indicating that the extent of bond formation in the transition state is moderate.

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