6279-34-1 Usage
Benzene derivative
The compound is derived from benzene, which means it is a chemical structure that has a benzene ring as its base or core.
Bromine atom at position 1
The compound has a bromine atom attached to the first carbon atom of the benzene ring, which can influence its reactivity and properties.
2-[(4-methylphenoxy)methyl] group at position 2
A substituent group consisting of a 4-methylphenoxy attached to a methyl group is attached to the second carbon atom of the benzene ring, further affecting the compound's properties and reactivity.
Commonly used in organic synthesis
The compound is frequently employed as a building block or intermediate in the synthesis of more complex organic molecules.
Utilized as a reagent
1-bromo-2-[(4-methylphenoxy)methyl]benzene can participate in various chemical reactions, making it a valuable tool in the field of chemistry.
Potential applications in pharmaceutical and agrochemical industries
The compound may have uses in the development of new drugs or agrochemicals due to its unique structure and reactivity.
Specific properties and uses vary
The exact properties and applications of 1-bromo-2-[(4-methylphenoxy)methyl]benzene depend on the specific requirements and goals of the synthesis or process in which it is used.
Check Digit Verification of cas no
The CAS Registry Mumber 6279-34-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,2,7 and 9 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 6279-34:
(6*6)+(5*2)+(4*7)+(3*9)+(2*3)+(1*4)=111
111 % 10 = 1
So 6279-34-1 is a valid CAS Registry Number.
6279-34-1Relevant articles and documents
Impregnated palladium on magnetite as catalyst for direct arylation of heterocycles
Cano, Rafael,Pérez, Juana M.,Ramón, Diego J.,McGlacken, Gerard P.
, p. 1043 - 1050 (2016/07/06)
Palladium impregnated on magnetite is an efficient, cheap and easy to prepare catalyst for the direct arylation of heterocycles. Good yields are afforded under relatively mild conditions and a broad substrate scope is evident. The catalyst is regioselective in many cases, affording arylated products, at the C2- or C3-position (depending of the heterocycle used). The methodology can be extended to prepare chromenes through an intramolecular direct arylation reaction. Some evidence is provided for two catalyst deactivation pathways, which prevents efficient recycling.
Biaryl synthesis via direct arylation: Establishment of an efficient catalyst for intramolecular processes
Campeau, Louis-Charles,Parisien, Mathieu,Leblanc, Melissa,Fagnou, Keith
, p. 9186 - 9187 (2007/10/03)
In this Communication, we describe direct arylation reactions with improved scope and catalyst activity for the intramolecular formation of biaryl compounds. This was achieved through the establishment of a highly active and robust catalyst system and the subsequent development of a novel phosphine ligand 27. The enhanced catalytic activity extends these transformations to include previously unreactive and poorly reactive substrates, and allows for very low catalyst loadings to be employedas little as 0.1 mol %. Copyright