135484-76-3

Usage

Uses

Used in Pharmaceutical Industry:
BENZOIC ACID, 2-BROMO-6-NITRO-, METHYL ESTER is used as an intermediate in the synthesis of various pharmaceuticals for its ability to contribute to the development of new drugs and medications.
Used in Agrochemical Industry:
In the agrochemical sector, BENZOIC ACID, 2-BROMO-6-NITRO-, METHYL ESTER is utilized as an intermediate in the production of agrochemicals, playing a role in the creation of substances that can protect crops and enhance agricultural productivity.
Used in Research and Development:
BENZOIC ACID, 2-BROMO-6-NITRO-, METHYL ESTER is employed as a building block in organic synthesis and as a reagent in chemical reactions within research and development, facilitating the exploration of new chemical compounds and processes.
Used in Organic Synthesis:
BENZOIC ACID, 2-BROMO-6-NITRO-, METHYL ESTER is used as a building block in organic synthesis for its capacity to be incorporated into the structures of more complex organic molecules, contributing to the advancement of chemical knowledge and the creation of novel substances.

Upstream product

• 38876-67-4 2-bromo-6-nitrobenzoic acid 
• 74-88-4 methyl iodide 
• 55289-35-5 2-bromo-6-nitrotoluene 
• 603-62-3 4-nitro-1H-isoindole-1,3(2H)-dione 
• 50573-74-5 6-nitroanthranilic acid 
• 65911-46-8 2-carbamoyl-6-nitrobenzoic acid 

Downstream Products

• 878159-99-0 methyl 2-allyl-6-nitrobenzoate 
• 878160-00-0 2-(3-hydroxy-propyl)-6-nitro-benzoic acid methyl ester 
• 878160-01-1 2-(2-carboxy-ethyl)-6-nitro-benzoic acid methyl ester 
• 878160-02-2 2-(2-methoxycarbonylamino-ethyl)-6-nitro-benzoic acid methylester 
• 878155-22-7 8-amino-2-methyl-3,4-dihydroisoquinolin-1-one 

Relevant academic research and scientific papers

Zn-Catalyzed Enantio- and Diastereoselective Formal [4 + 2] Cycloaddition Involving Two Electron-Deficient Partners: Asymmetric Synthesis of Piperidines from 1-Azadienes and Nitro-Alkenes

We report a catalytic asymmetric synthesis of piperidines through [4 + 2] cycloaddition of 1-azadienes and nitro-alkenes. The reaction uses earth abundant Zn as catalyst and is highly diastereo- and regioselective. A novel BOPA ligand (F-BOPA) confers high reactivity and enantioselectivity in the process. The presence of ortho substitution on the arenes adjacent to the bis(oxazolines) was found to be particularly impactful, due to limiting the undesired coordination of 1-azadiene to the Lewis acid and thus allowing the reaction to be carried out at lower temperature. A series of secondary kinetic isotope effect studies using a range of ligands implicates a stepwise mechanism for the transformation, involving an initial Michael-type addition of the imine to the nitro-alkene followed by a cyclization event. The stepwise mechanism obviates the electronic requirement inherent to a concerted mechanism, explaining the successful cycloaddition between two electron-deficient partners. (Chemical Equation Presented).

A microwave-assisted alternative synthesis of 8-amino-2-methyl-3,4- dihydroisoquinolin-1-one

A shorter, alternative synthesis of 8-amino-2-methyl-3,4- dihydroisoquinolin-1-one is described in 32% overall yield, over three steps starting from commercially available 2-methyl-6-nitrobenzonitrile. The synthesis includes two 'one-pot' procedures in wh

PYRIMIDINE DERIVATIVES

Novel pyrimidine derivatives of formula (I) to processes for their production, their use as pharmaceuticals and to pharmaceutical compositions comprising them.

Acid-catalysed Cyclisation of o-Sulphonamido Ketene Dithioacetal S-Oxides: A Novel Synthesis of the Indole Ring System

Treatment of o-sulphonamido aryl ketene dithioacetal S-oxides with hydrochloric acid in the presence of hydrogen sulphide gives 2-methylthioindoles.