3771-13-9

Usage

Uses

Used in Synthetic Organic Chemistry:
2-(Bromomethyl)-1-chloro-4-methoxybenzene is used as a building block for the synthesis of more complex organic molecules. Its functional groups allow for various chemical reactions, making it a valuable intermediate in the creation of new compounds.
Used in Pharmaceutical Research:
2-(Bromomethyl)-1-chloro-4-methoxybenzene is used as a starting material or intermediate in the development of new pharmaceuticals. Its unique structure and reactivity can be exploited to design and synthesize potential drug candidates, contributing to the advancement of medicinal chemistry.
Used in Chemical Research:
2-(Bromomethyl)-1-chloro-4-methoxybenzene is used as a research compound in academic and industrial laboratories. Its properties and reactivity can be studied to gain insights into the behavior of aromatic halides and their potential applications in various fields.

Upstream product

• 101252-66-8 (2-chloro-5-methoxyphenyl)methanol 
• 59-50-7 4-Chloro-3-methylphenol 
• 74-88-4 methyl iodide 
• 6280-89-3 2-chloro-5-methoxybenzoic acid 
• 54810-63-8 methyl (2-chloro-5-methoxy)benzoate 
• 100-84-5 1-methoxy-3-methyl-benzene 
• 13334-71-9 1-chloro-4-methoxy-2-methylbenzene 

Downstream Products

• 85970-53-2 2-(2-Benzenesulfinyl-2-fluoro-ethyl)-1-chloro-4-methoxy-benzene 
• 86001-96-9 2-(2-Benzenesulfinyl-2,2-dichloro-ethyl)-1-chloro-4-methoxy-benzene 
• 247569-87-5 N-(2-chloro-5-methoxybenzyl)phthalimide 
• 169045-07-2 2-{[4-chloro-3-(methyloxy)phenyl]methyl}-1H-isoindole-1,3(2H)-dione 
• 1256557-52-4 2-{[(2-chloro-5-methoxyphenyl)methyl]sulfanyl}-6-methylpyrimidin-4-ol 
• 90537-17-0 2-(2-chloro-5-methoxyphenyl)acetonitrile 
• 1274905-17-7 2-(2-chloro-5-methoxyphenyl)-2-isopropyl-3-methylbutanenitrile 
• 1274905-18-8 2-(2-chloro-5-hydroxyphenyl)-2-isopropyl-3-methylbutanenitrile 
• 1274905-19-9 2-(5-((2-bromobenzyl)oxy)-2-chlorophenyl)-2-isopropyl-3-methylbutanenitrile 
• 1274905-20-2 2-(2-chloro-((2-chlorobenzyl)oxy)phenyl)-2-isopropyl-3-methylbutanenitrile 
• 1274905-21-3 2-(5-((2-bromo-5-fluorobenzyl)oxy)-2-chlorophenyl)-2-isopropyl-3-methylbutanenitrile 
• 1274905-22-4 2-(5-((2-bromo-5-(trifluoromethyl)benzyl)oxy)-2-chlorophenyl)-2-isopropyl-3-methylbutanenitrile 
• 1274905-23-5 2-(5-((2-bromo-5-methoxybenzyl)oxy)-2-chlorophenyl)-2-isopropyl-3-methylbutanenitrile 
• 263840-73-9 3',5',6-trichloro-3,4'-dimethoxy-bibenzyl 

Relevant academic research and scientific papers

Synthesis of polycyclic molecules by double C(sp2)-H/C(sp 3)-H arylations with a single palladium catalyst

Polycyclic molecules were obtained in good yields by double C(sp 2)-H/C(sp3)-H arylations mediated by a single palladium/phosphine catalyst. Both double intermolecular/intramolecular and intramolecular/intramolecular C-C couplings we

METHYL SULFANYL PYRMIDMES USEFUL AS ANTIINFLAMMATORIES, ANALGESICS, AND ANTIEPILEPTICS

The present invention relates to pyrimidine derivatives of Formula (Ia) and (Ib) (including tautomers, isomers, prodrugs, and pharmaceutically acceptable salts thereof). Said compounds are useful in the treatment of pain (such as neuropathic pain), inflammation, and epilepsy (by acting as anticonvulsants). Methods of medical treatment making use of said compounds, as well as additional compounds of Formula (IIa) and (IIb), are also disclosed.

1-(2,6-Dichloro-4-hydroxyphenyl)-2-phenylethanes - New biological response modifiers for the therapy of breast cancer. Synthesis and evaluation of estrogenic/antiestrogenic properties

[meso-1,2-bis(2,6-dichloro-4-hydroxyphenyl)ethylenediamine]platinum(II) complexes (meso-1-ptll′; L,l′= Cl orL = H2O and L′ = OSO3) are highly effective towards hormone-sensitive, rodent breast cancers due to their significant estroge

Chemical and in vitro syntheses of brominated and chlorinated 3,4′-dihydroxybibenzyls (halogenated lunularins)

Ten halogenated lunularins 16, 17, 26, 27, 30, 31, 36, 37, 42 and 43 as model substances for a new class of halometabolites isolated from bryophytes are prepared by chemical total syntheses according to a Wittig-protocol using halogenated aldehydes and ph

Fullerene tectonics. Part 2. Synthesis and pyrolysis of halogenated benzo[c]phenanthrenes

Halogenated benzo[c]phenanthrenes with a halogen in the hindered fiord region are prepared by the photochemical cyclisation of appropriately substituted stilbenes. Pyrolysis gives the corresponding benzo[ghi]fluoranthrenes in moderate yields. At higher temperatures a competing rearrangement pathway to cyclopenta[cd]pyrene occurs.

Tetraisoquinoline compounds which have useful pharmaceutical utility

Tetrahydroisoquinoline compounds of formula I STR1 and pharmaceutically acceptable salts and lipophilic ester thereof have utility as analgesics and in the treatment of psychoses, Parinson''s disease, Lesch-Nyan syndrome, attention deficit disorder or cognitive impairment or in the relief of drug dependence or tardive dyskinesia.