151446-28-5

Basic information

• Product Name: 2-amino-3-bromo-5-methylbenzaldehyde
• Synonyms: 2-amino-3-bromo-5-methylbenzaldehyde
• CAS NO: 151446-28-5
• Molecular Formula: C₈H₈BrNO
• Molecular Weight: 214.05922
• Mol File: 151446-28-5.mol
• Article Data: 7

Chemical Properties

• Appearance: /
• Storage Temp.: 2-8°C
• CAS DataBase Reference: 2-amino-3-bromo-5-methylbenzaldehyde(CAS DataBase Reference)
• NIST Chemistry Reference: 2-amino-3-bromo-5-methylbenzaldehyde(151446-28-5)
• EPA Substance Registry System: 2-amino-3-bromo-5-methylbenzaldehyde(151446-28-5)

Safety Data

• Hazardous Substances Data: 151446-28-5(Hazardous Substances Data)

Usage

General Description

2-Amino-3-bromo-5-methylbenzaldehyde is a chemical compound with the molecular formula C8H8BrNO. It is an aromatic compound that contains a benzene ring with a bromine atom and a methyl group attached to it. The compound also has an aldehyde functional group and an amino group, which gives it both reactive and basic properties. 2-Amino-3-bromo-5-methylbenzaldehyde has potential applications in organic synthesis, pharmaceuticals, and material science due to its unique chemical structure and reactivity. It can be used as a building block in the synthesis of various organic compounds and pharmaceuticals, and its functional groups make it a useful reagent for chemical reactions such as nucleophilic substitution and condensation reactions.

Upstream product

• 13091-43-5 2-amino-3-bromo-5-methylbenzoic acid 
• 206551-32-8 methyl 2-amino-3-bromo-5-methyl benzoate 
• 55414-71-6 (2-amino-3-bromo-5-methylphenyl)methanol 
• 41825-73-4 2-bromo-4,6-dimethylaniline 

Relevant articles and documents

Chiral Phosphoric-Acid-Catalyzed Cascade Prins Cyclization

Asymmetric Prins cyclization of in situ generated quinone methides and o-aminobenzaldehyde has been developed with chiral phosphoric acid as an efficient catalyst. This unconventional method provides a facile access to diverse functionalized trans-fused pyrano-/furo-tetrahydroquinoline derivatives in excellent yield and with excellent diastereo- and enantioselectivities (up to 99% yield and 99% ee). Mechanistic studies suggested that the three adjacent tertiary stereocenters were constructed through the sequential formation of C-O, C-C, and C-N bonds.

BICYCLIC HETEROARYL SUBSTITUTED COMPOUNDS

Disclosed are compounds of Formula (I) to (IV): [INSERT CHEMICAL STRUCTURE HERE] or a stereoisomer, tautomer, pharmaceutically acceptable salt, solvate or prodrug thereof. Also disclosed are methods of using such compounds as PAR4 inhibitors, and pharmace

BENZOPYRAN COMPOUNDS USEFUL FOR TREATING INFLAMMATORY CONDITIONS

The subject invention concerns methods and compounds that have utility in the treatment of a condition associated with cyclooxygenase-2 mediated disorders. Compounds of particular interest are benzopyrans and their analogs defined by formula (1). Wherein Z, X, R1, R2, R3, and R4 are as described in specification.