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4-(2-chlorophenyl)pyridine is an organic compound characterized by its chemical formula C11H8ClN. It features a pyridine ring, which is a six-membered aromatic ring containing one nitrogen atom, and a chlorophenyl group, which is a benzene ring with one chlorine atom attached. The chlorine atom is located at the 2-position of the phenyl ring, and this group is attached to the 4-position of the pyridine ring. 4-(2-chlorophenyl)pyridine is a white to off-white crystalline solid and is used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals due to its potential to form diverse chemical structures. It is important to handle 4-(2-chlorophenyl)pyridine with care, as it may have toxicological properties and requires proper safety measures during its use and disposal.

4467-15-6

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4467-15-6 Usage

Chemical compound

4-(2-chlorophenyl)pyridine

Physical state

Pale yellow solid

Uses

Building block in organic synthesis, precursor in pharmaceutical and agrochemical production, development of materials with optoelectronic and photophysical properties

Aromatic properties

Known for its aromatic properties

Commonly utilized in

Synthesis of heterocyclic compounds

Handling precautions

Important to handle with care to avoid risks to human health and the environment

Check Digit Verification of cas no

The CAS Registry Mumber 4467-15-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,4,6 and 7 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 4467-15:
(6*4)+(5*4)+(4*6)+(3*7)+(2*1)+(1*5)=96
96 % 10 = 6
So 4467-15-6 is a valid CAS Registry Number.

4467-15-6Downstream Products

4467-15-6Relevant academic research and scientific papers

Palladium-Catalyzed Electrophilic Functionalization of Pyridine Derivatives through Phosphonium Salts

Che, Yuan-Yuan,Deng, Xuezu,Feng, Chao,Lin, Ling-Zhi,Pei, Bingbing,Yue, Yanni

supporting information, p. 16414 - 16419 (2020/07/20)

Herein, we report a highly efficient and practical method for pyridine-derived heterobiaryl synthesis through palladium-catalyzed electrophilic functionalization of easily available pyridine-derived quaternary phosphonium salts. The nice generality of this reaction was goes beyond arylation, enabling facile incorporation of diverse carbon-based fragments, including alkenyl, alkynyl, and also allyl fragments, onto the pyridine core. Notably, the silver salt additive is revealed to be of vital importance for the success of this transformation and its pivotal role as transmetallation mediator, which guarantees a smooth transfer of pyridyl group to palladium intermediate, is also described.

Synthesis of Vinylphenylpyridine and Living Anionic Polymerization

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Page/Page column 7, (2009/05/29)

Provided are a vinyl-biphenylpyridine monomer and a polymer thereof. More particularly, the present invention provides a vinyl-biphenylpyridine monomer having a side chain of pyridine or phenylpyridine as a functional group, a homopolymer of which molecul

SYNTHESIS OF VINYLPHENYLPYRIDINE AND LIVING ANIONIC POLYMERIZATION

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Page/Page column 10, (2010/11/29)

Provided are a vinyl-biphenylpyridine monomer and a polymer thereof. More particularly, the present invention provides a vinyl-biphenylpyridine monomer having a side chain of pyridine or phenylpyridine as a functional group, a homopolymer of which molecul

THE PYRIDYL CATION AS A REACTIVE INTERMEDIATE IN THE PHOTOREACTION OF IODOPYRIDINES WITH BENZENES

Ohkura, Kazue,Seki, Koh-ichi,Terashima, Masanao,Kanaoka, Yuichi

, p. 3433 - 3436 (2007/10/02)

The electrophilic behavior of the reactive entity in the photosubstitution of benzenes with 2-iodopyridine was found to be ascribable to the intermediary 2-pyridyl cation, rather than the electrophilic 2-pyridyl radical.

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