17100-65-1

Usage

Uses

Used in Pharmaceutical Industry:
Methyl 2-bromo-4-methoxybenzoate is used as an intermediate in the synthesis of pharmaceuticals for its ability to contribute to the development of new drugs and improve existing ones.
Used in Agrochemical Industry:
In the agrochemical industry, Methyl 2-bromo-4-methoxybenzoate is utilized as an intermediate in the production of agrochemicals, aiding in the creation of more effective and safer products for agricultural applications.
Used in Specialty Chemicals Industry:
Methyl 2-bromo-4-methoxybenzoate is employed as an intermediate in the synthesis of specialty chemicals, contributing to the development of unique and high-quality chemical products for various applications.
Used as a Reagent in Organic Synthesis:
Methyl 2-bromo-4-methoxybenzoate is used as a reagent in the preparation of various esters and ethers, facilitating the synthesis of a wide range of organic compounds.
It is important to handle Methyl 2-bromo-4-methoxybenzoate with caution due to its potential for skin and eye irritation, and it should be stored and used in accordance with proper safety protocols.

InChI:InChI=1/C9H9BrO3/c1-12-6-3-4-7(8(10)5-6)9(11)13-2/h3-5H,1-2H3

Upstream product

• 16426-64-5 2-bromo-4-nitrobenzoic acid 
• 98545-64-3 methyl-2-bromo-4-aminobenzoate 
• 100959-22-6 methyl 2-bromo-4-nitrobenzoate 
• 101085-03-4 2-bromo-4-hydroxybenzoic acid methyl ester 
• 74-88-4 methyl iodide 
• 89691-67-8 1-(2-bromo-4-methoxyphenyl)ethanone 
• 2398-37-0 3-methoxyphenyl bromide 
• 67-56-1 methanol 
• 74317-85-4 2-bromo-4-methoxybenzoic acid 

Downstream Products

• 1440546-79-1 methyl 2-((2-amino-5-methoxyphenyl)ethynyl)-4-methoxybenzoate 
• 121-98-2 methyl 4-methoxybenzoate 
• 1440546-80-4 2-((2-Acetamido-5-methoxyphenyl)ethynyl)-4-methoxybenzoic acid 
• 1440546-89-3 methyl 2-((2-acetamido-5-methoxyphenyl)ethynyl)-4-methoxybenzoate 
• 1440546-78-0 2-((2-acetamido-5-methoxyphenyl)ethynyl)-4-methoxy-N-methylbenzamide 
• 101085-03-4 2-bromo-4-hydroxybenzoic acid methyl ester 
• 931092-93-2 4-methoxy-2-vinylbenzoic acid methyl ester 

Relevant academic research and scientific papers

Atropisomeric bisoxazoline ligands with a bridge across the 5,5′-position of biphenyl for asymmetric catalysis

A new family of atropisomeric bisoxazoline ligands 2 with a bridge across the 5,5′-position of biphenyl has been developed. The axial chirality of this type of ligands can be retained by macro-ring strain produced by 5,5′-linkage of biphenyls even without

Highly enantioselective Pd(II)-catalyzed Wacker-type cyclization of 2-allylphenols by use of bisoxazoline ligands with axis-unfixed biphenyl backbone

A series of axis-unfixed bisoxazoline ligands with different steric and electronic properties has been synthesized. Due to the different steric interactions, the ligands afforded only one of the two possible diastereomeric Pd(II)-complexes upon metal coor

A-D-D ’ - A type asymmetric organic photovoltaic receptor material and application thereof

The invention belongs to the technical field of organic photovoltaic, and particularly relates to A-D-D ' - A asymmetric organic photovoltaic receptor material and application thereof. The framework containing the non-covalent bond configuration lock is j

AMINE COMPOUND FOR INHIBITING SSAO / VAP-1 AND USE THEREOF

An amine compound serving as a semicarbazide-sensitive amine oxidase (SSAO) and/or vascular adhesion protein-1 (VAP-1) inhibitor, a pharmaceutical composition, and an application thereof in medicines that can be used for treating inflammation and/or inflammation related diseases, diabetes and/or a disease related diabetes, psychiatric disorder, ischemic disease, vascular disease, fibrosis, or tissue transplant rejection.

COMPOUNDS AND METHODS FOR REGULATING INSULIN SECRETION

Disclosed herein are methods for inducing insulin secretion in a glucose-dependent manner and compounds for use in these methods.

cGAS ANTAGONIST COMPOUNDS

Disclosed are novel compounds of Formula (I) that are cGAS antagonists, methods of preparation of the compounds, pharmaceutical compositions comprising the compounds, and their use in medical therapy.

AMPHIPATHIC AND OTHER DOUBLE-SIDED ALPHA-HELIX MIMETICS BASED ON A 1,2-DIPHENYLACETYLENE SCAFFOLD

Small-molecule scaffolds based on 1,2-diphenylacetylene that accurately replicate the spatial and angular projections of several side chains on both faces of an α-helix, specifically the i and i+7 side chains on one face, and the i and i+2 side chains on the other. The amphipathic α-helix mimetic can be used to disrupt disease-promoting protein-protein interactions that are mediated by α-helices.

Amphipathic α-helix mimetics based on a 1,2-diphenylacetylene scaffold

In order to mimic amphipathic α-helices, a novel scaffold based on a 1,2-diphenylacetylene was designed. NMR and computational modeling confirmed that an intramolecular hydrogen bond favors conformations of the 1,2-diphenylacetylene that allow for accurat

SMALL MOLECULE COMPOUNDS FOR STEM CELL DIFFERENTIATION

Methods and small molecule compounds for stem cell differentiation are provided. One example of a class of compounds that may be used is represented by the compound having the structure IA or IB in the form of free base or a pharmaceutically acceptable salt, hydrate, solvate or N-oxide thereof. R1 is independently hydrogen or (C1-C6)alkyl; R2 is independently hydrogen, (C1-C6)alkyl, aryl, or heteroaryl; R2' is independently hydrogen, (C1-C6)alkyl, CF3 or C2F5; R3 is independently (C1-C6)alkyl, aryl, 2-tetrahydrofuryhnethyl, an aliphatic tertiary amine, or 4-methoxybenzyl; or R2 and R3 may be joined together to form a 5 or 6 member ring lactone; R4 is independently hydrogen, (C1-C6)alkyl, a 2- or 4-R5-substituted aromatic ring selected from a 4-R5-phenyl or a 2-R5-5-pyridyl, aryl, heteroaryl, aliphatic tertiary amine or halogen; and R5, R5', R6, R6', R7, R7' are each independently hydrogen, (C1-C6)alkyl, aryl, optionally substituted phenyl, heteroaryl, a heterocyclic ring, an aliphatic tertiary amine, or halogen.

5,5'- POSITION LINKED 1,1'- BIPHENYL AXIAL CHIRAL LIGAND AND METHOD FOR PREPARING THE SAME

The present invention relates to a 5,5′-position linked 1,1′-biphenyl axis chiral ligand in chemical industry field. The present invention incorporates both the central chirality of oxazoline and the axial chirality of diphenyls. Such ligand can be used i