338385-91-4

Usage

Uses

Used in Pharmaceutical Industry:
2-(5-bromo-2-methoxyphenyl)propan-2-ol is used as a chiral building block for the synthesis of various pharmaceuticals, contributing to the development of new drugs with improved efficacy and selectivity.
Used in Agrochemical Industry:
In the agrochemical industry, 2-(5-bromo-2-methoxyphenyl)propan-2-ol is utilized as a key intermediate in the production of agrochemicals, enhancing the effectiveness of pesticides and other agricultural chemicals.
Used in Fragrance Industry:
2-(5-bromo-2-methoxyphenyl)propan-2-ol is employed as a component in the creation of fragrances, adding unique scents and improving the overall quality of perfumes and other scented products.
Used in Dye Industry:
2-(5-bromo-2-methoxyphenyl)propan-2-ol is used in the dye industry as a precursor for the synthesis of various dyes, contributing to the development of new colorants with improved properties and applications.
Used in Organic Chemistry Research:
In the field of organic chemistry research, 2-(5-bromo-2-methoxyphenyl)propan-2-ol serves as a valuable tool for the exploration of new chemical reactions and processes, furthering scientific understanding and innovation.

Upstream product

• 1638291-19-6 5-bromo-2-methoxy-N-methyl-N-(4-methylbenzenesulfonyl)benzenecarboxamide 
• 75-16-1 methylmagnesium bromide 
• 630050-32-7 3-bromo-N-(4-methylbenzenesulfonyl)benzenecarboxamide 
• 1638287-10-1 5-bromo-2-methoxy-N-(4-methylbenzenesulfonyl)benzenecarboxamide 
• 1711-09-7 3-bromobenzoyl chloride 
• 2476-35-9 5-bromo-2-methoxybenzoic acid 
• 7120-41-4 methyl 5-bromo-2-methoxybenzoate 
• 74-88-4 methyl iodide 

Downstream Products

• 1443151-90-3 2-[2-methoxy-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]propan-2-ol 
• 1443151-66-3 2-[5-(4-{[2-(4-fluorophenyl)ethyl]amino}-6-methoxy-1,3,5-triazin-2-yl)-2-methoxyphenyl]propan-2-ol 
• 1443151-80-1 2-{5-[4-(Fluoromethoxy)-6-{[2-(4-fluorophenyl)ethyl]amino}-1,3,5-triazin-2-yl]-2-methoxyphenyl}propan-2-ol 
• 1443152-04-2 tert-butyl {4-(Fluoromethoxy)-6-[3-(1-hydroxy-1-methylethyl)-4-methoxyphenyl]-1,3,5-triazin-2-yl}[2-(4-fluorophenyl)ethyl]carbamate 
• 1443152-03-1 tert-butyl [2-(4-fluorophenyl)ethyl]{4-hydroxy-6-[3-(1-hydroxy-1-methylethyl)-4-methoxyphenyl]-1,3,5-triazin-2-yl}carbamate 
• 1443152-02-0 4-{[2-(4-fluorophenyl)ethyl]amino}-6-[3-(1-hydroxy-1-methylethyl)-4-methoxyphenyl]-1,3,5-triazin-2-ol 

Relevant academic research and scientific papers

Room-temperature ortho-alkoxylation and -halogenation of N-tosylbenzamides by using palladium(II)-catalyzed C-H activation

The N-tosylcarboxamide group can direct the room-temperature palladium-catalyzed C-H alkoxylation and halogenation of substituted arenes in a simple and mild procedure. The room-temperature stoichiometric cyclopalladation of N-tosylbenzamide was first studied, and the ability of the palladacycle to react with oxidants to form C-X and C-O bonds under mild conditions was demonstrated. The reaction conditions were then adapted to promote room-temperature ortho-alkoxylations and ortho-halogenations of N-tosylbenzamides using palladium as catalyst. The scope and limitation of both alkoxylations and halogenations was studied and the subsequent functional transformation of the N-tosylcarboxamide group through nucleophilic additions was evaluated. This methodology offers a simple and mild route to diversely functionalized arenes.

1,3,5-TRIAZINE-2-AMINE DERIVATIVES, PREPARATION THEREOF AND DIAGNOSTIC AND THERAPEUTIC USE THEREOF

The present invention relates to compounds corresponding to formula (I) in which: - R1 represents a substituted phenyl; - R2 represents: - a substituted phenyl; - a heteroaromatic group, the said group being unsubstituted or substituted one or more times; - R3 represents a group Alk; - R4 represents a hydrogen atom or a (C1-C4)alkyl; - R5 represents a hydrogen atom, a (C3-C6)cycloalkyl or a (C1-C4)alkyl-O-Alk; - or alternatively R4 and R5, together with the nitrogen atom to which they are attached, constitute a heterocyclic radical chosen from: azetidin-1-yl, pyrrolidin-1-yl, piperid-1-yl, morpholin-4-yl; - R6 represents a group -COOAlk, a group -CONH2 or a group -NHSO2 Alk; - Alk represents a (C1-C4)alkyl, which is unsubstituted or substituted one or more times with a halogen atom; in the form of the base or of an acid-addition salt. Preparation process and diagnostic and therapeutic use