35446-28-7

Usage

Explanation

This is the common name used to describe the compound, which is derived from its structure and the functional groups present.

Explanation

The compound is a derivative of acetophenone, which means it is structurally similar to acetophenone but has additional functional groups or modifications.

Explanation

The bromine atom is attached to the second carbon atom in the molecule, which is part of the acetophenone structure.

Explanation

The methoxy group (-OCH3) is attached to the fourth carbon atom of the phenyl ring, which is part of the acetophenone structure.

Explanation

The compound is used as a starting material or intermediate in various organic synthesis reactions, which involve the formation of new chemical bonds and the creation of new compounds.

Explanation

The compound is used in pharmaceutical research, which involves the study of drugs and their effects on living organisms.

Explanation

The compound serves as a building block or precursor in the synthesis of other compounds, contributing to the formation of more complex molecules.

Explanation

The compound's structure includes a bromine atom, a methoxy group, and a methyl group, which are all attached to the acetophenone backbone. These functional groups give the compound its unique properties and reactivity.

Derivative of

Acetophenone

Bromine Attachment

Second carbon

Methoxy Group Attachment

Fourth carbon of the phenyl ring

Usage

Organic synthesis reactions

Application

Pharmaceutical research

Role

Building block in the production of other compounds

Structure

Contains a bromine atom, a methoxy group, and a methyl group

Upstream product

• 82938-20-3 3-methyl-1-(4-methoxyphenyl)-1-butanone 

Downstream Products

• 116849-91-3 2-Isopropyl-3-(4-methoxy-phenyl)-2H-thiochromene 
• 873440-69-8 5-isopropyl-4-(4-methoxyphenyl)-2-methylthiazole 
• 612824-87-0 (±)-2-azido-1-(4-methoxyphenyl)-3-methylbutan-1-one 

Relevant academic research and scientific papers

Catalytic Lewis and Br?nsted acid syn-diastereoselective benzylic substitutions of α-hydroxy-β-nitro- and α-hydroxy-β-azido-alkyl arenes

A series of alkyl and alkenyl p-methoxy arenes containing α,β-disubstituted diamino and amino alcohol groups were synthesized from β-nitro and β-azido benzylic alcohols in the presence of AuCl3 as catalyst. The formation of predominantly syn-disubstituted products were rationalized on the basis of mechanistic considerations and transition state models relying on A1,3-allylic strain. The products could have utility in the design of medicinally relevant compounds and as chiral ligands for asymmetric catalysis. A new synthesis of (+)-sertraline (Zoloft) was achieved.

Kinetic diastereomer differentiation in Au(III)- and Bi(III)-catalyzed benzylic arylation: Concise and stereocontrolled synthesis of 2-amino-1,1-diarylalkanes

Benzylic alcohols carrying an adjacent α-nitro or α-azido group on the alkane chain are converted into syn-1,1-diaryl-2-nitro- and 2-azidoalkanes with electron-rich arenes in stereoselective reactions catalyzed by Bronsted and Lewis acids. Gold(III) chloride and bismuth(III) triflate were found to be especially efficient as catalysts, showing kinetically controlled differentiation in the reactivity of diastereomeric α-substituted benzyl alcohols. Applications to therapeutically relevant syn- and anti- 2-amino-1,1-diarylalkanes are projected.

AN IMPROVED PROCESS FOR PREPARING N-HYDROXY-4-{5- [4- (5-ISOPROPYL-2-METHYL-l, 3-THIAZOL-4-YL) -PHENOXY] -PENTOXY }-BENZAMIDINE

This invention relates to an improved method of preparing N-hydroxy-4-{5- [4- (5-isopropyl-2-methyl-l, 3-thiazol-4-yl) phenoxy] pentoxy }benzamidine .