36449-75-9

Usage

Uses

Used in Perfumery Industry:
2-Methoxyphenethyl Bromide is used as a fragrance ingredient for its pleasant odor, contributing to the creation of various scents in perfumes.
Used in Pharmaceutical Industry:
2-Methoxyphenethyl Bromide is used as a chemical intermediate in the synthesis of pharmaceutical compounds, taking advantage of its alkylating agent properties.
Used in Organic Synthesis:
2-Methoxyphenethyl Bromide is used as a reagent in organic synthesis applications, where its reactivity plays a crucial role in the formation of new chemical entities.

Upstream product

• 31949-21-0 bromomethyl 2-methoxyphenyl ketone 
• 27798-60-3 methyl 2-(2-methoxyphenyl)acetate 
• 614-75-5 2-Hydroxyphenylacetic acid 
• 1122-58-3 dmap 
• 7417-18-7 2-methoxyphenethyl alcohol 
• 124-63-0 methanesulfonyl chloride 
• 121-44-8 triethylamine 
• 558-13-4 carbon tetrabromide 
• 93-25-4 2-methoxyphenylacetic acid 

Downstream Products

• 411237-43-9 (2-methoxy-phenethyl)-malonic acid diethyl ester 
• 145851-06-5 3-(2-methoxyphenyl)propanenitrile 
• 123060-84-4 ethyl 3-(o-methoxyphenylethyl)-2-methyl-4-oxocyclohex-2-encarboxylate 
• 52093-69-3 5-(2-methoxyphenyl)-1-pentene 
• 79146-45-5 2-[2-(2-Methoxy-phenyl)-ethyl]-isothiourea; hydrobromide 
• 159835-84-4 3-hydroxy-3-methyl-5-(o-methoxyphenyl)pent-1-ene 
• 1376605-95-6 1-(2-methoxyphenethyl)-4-decyl-1H-1,2,3-triazole 
• 1376605-96-7 1-(2-methoxyphenethyl)-4-dodecyl-1H-1,2,3-triazole 
• 823189-07-7 1-(2-azidoethyl)-2-methoxybenzene 
• 185760-63-8 2-[2-(2'-methoxyphenyl)-ethyl]-2-cyclohexen-1-one 
• 33209-75-5 4-(2-Methoxyphenyl)-butanoic acid 
• 73735-41-8 1-(4-fluorobenzyl)-N-(1-(2-methoxyphenethyl)piperidin-4-yl)-1H-benzo[d]imidazol-2-amine 
• 2045-79-6 o-methoxy-2-phenylethylamine 

Relevant academic research and scientific papers

BISPHENOLATE TRANSITION METAL COMPLEXES, PRODUCTION AND USE THEREOF

Bis phenolate transition metal complexes are disclosed for use in alkene polymerization, with optional chain transfer agent, to produce polyolefins.

Iron-catalyzed borylation of alkyl, allyl, and aryl halides: Isolation of an iron(I) boryl complex

Activation of B2pin2 with tBuLi facilitates the Fe-catalyzed borylation of alkyl, allyl, benzyl, and aryl halides via the formation of Li[B2pin2(tBu)] (1). The reaction of 1 with a representative iron phosphine precatalyst generates the unique iron(I) boryl complex [Fe(Bpin)(dpbz)2] (2).

NOVEL THIOPHENE DERIVATIVES AS IMMUNOSUPPRESSIVE AGENTS

The invention relates to novel thiophene derivatives, their preparation and their use as pharmaceutically active compounds. Said compounds particularly act as immunosuppressive agents.

NOVEL THIOPHENE DERIVATIVES

The invention relates to novel thiophene derivatives, their preparation and their use as pharmaceutically active compounds. Said compounds particularly act as immunosuppressive agents.

Imidazopyridinone derivatives and their use as phosphodiesterase inhibitors

A compound (Ia): wherein the variables are defined in the specification, its prodrug or a pharmaceutically acceptable salt thereof useful in the treatment of angina, hypertension etc.

Tetracyclic triterpene derivatives with immunosuppressant activity

The compounds of Formula I are useful as immunosuppressive agents.

Diastereoselective intramolecular meta photocycloaddition of side-chain- substituted 5-(2-methoxyphenyl)pent-1-enes

Irradiation of a series of 5-(2-methoxyphenyl)pent-1-enes substituted with a hydroxy or trimethylsilyloxy group at the α-, β-, or γ-position of the side-chain yields in all cases meta photocycloadducts, in which the configuration at the substituted carbon atom is mainly endo. This indicates that the diastereoselectivity originates from minimization of steric interactions between the side-chain substituent and the ortho-methoxy group at the arene unit. Hydrogen bonding does not seem to be involved. The introduction of the side-chain substituents also influences the regioselectivity of the addition: The linear to angular adduct ratios are significantly increased compared to the case of the parent compound.