Zheng, Lvyin team published research in Organic Chemistry Frontiers in 2022 | 6911-87-1

6911-87-1, 4-Bromo-N-methylaniline is a aniline based compound known to exhibit mutagenic properties.
4-Bromo-N-methylaniline is a useful research compound. Its molecular formula is C7H8BrN and its molecular weight is 186.05 g/mol. The purity is usually 95%.
4-Bromophenylmethylamine is an organic compound that has anti-inflammatory properties and is used as a pharmaceutical. It belongs to the group of amines. The hydrolysis of 4-bromophenylmethylamine by hydrochloric acid produces phenol and bromamine (NHBr). The reaction system can be used to synthesize a number of compounds, including anilines, benzofurans, and other aromatic compounds. 4-Bromophenylmethylamine reacts with muscle tissue in a similar manner as acetaminophen does. This drug also has been shown to have significant effects on the energy metabolism in the muscles of rats that are given carbon source., Application of C7H8BrN

Organic bromides such as alkyl bromides are used as fumigants in agriculture to control insects. 6911-87-1, formula is C7H8BrN, Name is 4-Bromo-N-methylaniline. Ethylene bromide is one of the commercially important organic bromides which are the component of leaded gasoline. Application of C7H8BrN.

Zheng, Lvyin;Zhuo, Xiaoya;Wang, Yihan;Zou, Xiaoying;Zhong, Yumei;Guo, Wei research published 《 Photocatalytic cross-dehydrogenative coupling reaction toward the synthesis of N,N-disubstituted hydrazides and their bromides》, the research content is summarized as follows. N,N-Disubstituted hydrazides are useful synthetic building blocks and important pharmaceutical scaffolds in the fields of organo-pharmaceutical chem. Direct C(=O)-N-N bond formation represents one of the most effective strategies through a cross-dehydrogenative coupling (CDC) process. Here authors report an efficient method for the divergent synthesis of N,N-disubstituted hydrazides and their bromides from N,N-disubstituted hydrazines and aldehydes by photoredox-catalytic CDC reactions. This versatile protocol enables the direct construction of C(O)-N-N and C(sp2)-Br bonds simultaneously from available starting materials without prefunctionalization. This one-pot strategy shows the advantages of mild reaction conditions, high atom and step economy, high regioselectivity, as well as good functional group tolerance. In addition, the selected compounds exhibit potential antitumor activities as new chem. entities, thus showing potential applications in the field of new anticancer drug research.

6911-87-1, 4-Bromo-N-methylaniline is a aniline based compound known to exhibit mutagenic properties.
4-Bromo-N-methylaniline is a useful research compound. Its molecular formula is C7H8BrN and its molecular weight is 186.05 g/mol. The purity is usually 95%.
4-Bromophenylmethylamine is an organic compound that has anti-inflammatory properties and is used as a pharmaceutical. It belongs to the group of amines. The hydrolysis of 4-bromophenylmethylamine by hydrochloric acid produces phenol and bromamine (NHBr). The reaction system can be used to synthesize a number of compounds, including anilines, benzofurans, and other aromatic compounds. 4-Bromophenylmethylamine reacts with muscle tissue in a similar manner as acetaminophen does. This drug also has been shown to have significant effects on the energy metabolism in the muscles of rats that are given carbon source., Application of C7H8BrN

Referemce:
Bromide – Wikipedia,
bromide – Wiktionary