719310-30-2

Usage

Uses

Used in Organic Synthesis:
(5-Bromo-2-hydroxyphenyl)carbamic acid tert-butyl ester is used as a synthetic intermediate for the preparation of various organic compounds. Its unique structure allows for versatile chemical reactions, enabling the synthesis of a wide range of molecules with potential applications in different industries.
Used in Pharmaceutical Research:
In the pharmaceutical industry, (5-Bromo-2-hydroxyphenyl)carbamic acid tert-butyl ester is used as a starting material or building block for the development of new drugs. Its chemical properties and functional groups can be utilized to create novel drug candidates with potential therapeutic effects.
Used in the Development of New Materials:
(5-Bromo-2-hydroxyphenyl)carbamic acid tert-butyl ester may also find applications in the development of new materials, such as polymers, coatings, or adhesives. Its unique structure and functional groups can contribute to the creation of materials with specific properties, such as improved stability, adhesion, or reactivity.

Upstream product

• 24424-99-5 di-tert-butyl dicarbonate 
• 40925-68-6 2-amino-4-bromo-phenol 

Downstream Products

• 719310-31-3 tert-butyl 6-bromo-2,3-dihydrobenzo[b][1,4]oxazine-4-carboxylate 

Relevant academic research and scientific papers

ANTIBACTERIAL COMPOUNDS

The present invention relates to compounds of general formula (II),to compositions comprising these compounds and to methods of treating Enterobacteriaceae bacterial diseases and infections using the compounds. The compounds find application in the treatment of infection with, and diseases caused by, Enterobacteriaceae.

Syntheses and kinetic studies of cyclisation-based self-immolative spacers

Kinetic analysis of the disassembly of self-immolative spacers based on cyclisation processes was performed. Five compounds were synthesized belonging to two different series, and their kinetic constants were determined. Electron-donating substituents gav

Enantioselective Synthesis of 2,3-Disubstituted Benzomorpholines: Analogues of Lignan Natural Products

The enantioselective synthesis of 2,3-disubstituted benzomorpholines, analogues of 1,4-benzodioxane natural products, has been achieved via addition of electron-rich aromatic donors to acyl-iminium ions derived from benzomorpholine aminols. Subsequent mod

BENZOXAZINES AND DERIVATIVES THEREOF AS INHIBITORS OF PI3KS

The present invention provides compounds of Formula (I) wherein W, Q, E, D, A, L, R6, R7, R8, Y, K, R9, R10,G, the dashed bond between D and E, and the double bond denoted "*" have any of the values defined therefore in the specification, and pharmaceutically acceptable salts thereof, that are useful as agents in the treatment of diseases and conditions, including inflammatory diseases, cardiovascular diseases, and cancers. Also provided are pharmaceutical compositions comprising one or more compounds of Formula (I).