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2-(bromomethyl)-6-phenylpyridine is a chemical compound with the molecular formula C13H10BrN. It is a brominated derivative of the heterocyclic aromatic compound pyridine, featuring a benzyl group at the 2-position and a phenyl group at the 6-position. 2-(bromomethyl)-6-phenylpyridine is known for its versatile applications in various fields, including organic synthesis, pharmaceutical research, and material science.

864779-07-7

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864779-07-7 Usage

Uses

Used in Organic Synthesis:
2-(bromomethyl)-6-phenylpyridine is used as a key intermediate in organic synthesis for the preparation of various functionalized pyridine derivatives. Its unique structure allows for further chemical modifications, making it a valuable building block in the synthesis of complex organic molecules.
Used in Pharmaceutical Research:
In the pharmaceutical industry, 2-(bromomethyl)-6-phenylpyridine is utilized as a starting material for the development of new drugs. Its ability to form various functionalized pyridine derivatives makes it a promising candidate for the design of novel therapeutic agents with potential applications in treating various diseases.
Used in Agrochemicals:
2-(bromomethyl)-6-phenylpyridine is also employed in the development of agrochemicals, such as pesticides and herbicides. Its potential antifungal and antibacterial properties make it a valuable component in the creation of effective crop protection products.
Used in Materials Science:
In the field of materials science, 2-(bromomethyl)-6-phenylpyridine has been investigated for its potential applications in the synthesis of functional materials. Its unique structure and properties can contribute to the development of advanced materials with specific characteristics, such as conductivity, magnetism, or catalytic activity.
Used in Catalysis:
2-(bromomethyl)-6-phenylpyridine has been studied as a potential catalyst or catalyst precursor in various chemical reactions. Its ability to form stable complexes with metal ions and its reactivity make it a promising candidate for use in catalytic processes, enhancing the efficiency and selectivity of chemical transformations.

Check Digit Verification of cas no

The CAS Registry Mumber 864779-07-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,4,7,7 and 9 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 864779-07:
(8*8)+(7*6)+(6*4)+(5*7)+(4*7)+(3*9)+(2*0)+(1*7)=227
227 % 10 = 7
So 864779-07-7 is a valid CAS Registry Number.

864779-07-7Relevant academic research and scientific papers

HETEROCYCLIC COMPOUND AND USE THEREOF

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, (2019/02/15)

The present invention provides a heterocyclic compound having an orexin type 2 receptor agonist activity. A compound represented by the formula (I) : wherein each symbol is as described in the specification, or a salt thereof, is useful as an agent for the prophylaxis treatment of narcolepsy.

Rhodium(I) Complexes with Ligands Based on N-Heterocyclic Carbene and Hemilabile Pyridine Donors as Highly e Stereoselective Alkyne Hydrosilylation Catalysts

Morales-Cerón, Judith P.,Lara, Patricia,López-Serrano, Joaquín,Santos, Laura L.,Salazar, Verónica,álvarez, Eleuterio,Suárez, Andrés

supporting information, p. 2460 - 2469 (2017/07/17)

Cationic rhodium(I) complexes containing picolyl-NHC (NHC = N-heterocyclic carbene) ligands that differ in the substitution at the 6-position of the pyridine donor serve as efficient E-selective alkyne hydrosilylation catalyst precursors. Particularly, wh

Chiral, Sterically Demanding N-Heterocyclic Carbenes Fused into a Heterobiaryl Skeleton: Design, Synthesis, and Structural Analysis

Espina, Manuela,Rivilla, Ivan,Conde, Ana,Díaz-Requejo, M. Mar,Pérez, Pedro J.,álvarez, Eleuterio,Fernández, Rosario,Lassaletta, José M.

, p. 1328 - 1338 (2015/04/27)

A series of Cu(I), Ag(I), and Au(I) complexes incorporating a new family of imidazopyridin-3-ylidene ligands substituted by a diphenylpyrrolidino group at N(1) and aryl groups at C(5) has been synthesized and their structures determined by X-ray diffracti

Atropoisomeric (P,N) ligands for the highly enantioselective Pd-catalyzed intramolecular asymmetric α-arylation of α-branched aldehydes

Nareddy, Pradeep,Mantilli, Luca,Guenee, Laure,Mazet, Clement

, p. 3826 - 3831 (2012/06/01)

Three-in-one: A short synthetic route readily gives access to a new class of chiral (P,N) ligands characterized by three distinct elements of chirality. These ligands are highly enantioselective in the challenging Pd-catalyzed intramolecular asymmetric α-

2-Alkyl nicotinoids and processes for their production

-

, (2008/06/13)

The invention relates to 2-alkyl nicotinoids and improved methods for producing them.

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