56256-14-5

Basic information

• Product Name: 4-BROMO-3-METHOXYBENZOIC ACID 98
• Synonyms: 4-Bromo-3-methoxybenzoic acid;2-Bromo-5-carboxyanisole;2-Bromo-5-carboxyanisole, 4-Bromo-m-anisic acid;56256-14-5;4-BROMO-3-METHOXYBENZOIC ACID 98;4-Bromo-3-methoxybenzoic acid 98%
• CAS NO: 56256-14-5
• Molecular Formula: C₈H₇BrO₃
• Molecular Weight: 231.04338
• Product Categories: blocks;Bromides;Carboxes;Acids & Esters;Anisoles, Alkyloxy Compounds & Phenylacetates;Bromine Compounds
• Mol File: 56256-14-5.mol
• Article Data: 19

Chemical Properties

• Melting Point: 221-224
• Boiling Point: 333.7 °C at 760 mmHg
• Flash Point: 155.6°C
• Appearance: /
• Density: 1.625g/cm³
• Vapor Pressure: 5.31E-05mmHg at 25°C
• Refractive Index: 1.583
• Storage Temp.: Keep Cold
• PKA: 3.85±0.10(Predicted)
• CAS DataBase Reference: 4-BROMO-3-METHOXYBENZOIC ACID 98(CAS DataBase Reference)
• NIST Chemistry Reference: 4-BROMO-3-METHOXYBENZOIC ACID 98(56256-14-5)
• EPA Substance Registry System: 4-BROMO-3-METHOXYBENZOIC ACID 98(56256-14-5)

Safety Data

• Hazard Codes: Xi
• RIDADR: UN2811
• Hazardous Substances Data: 56256-14-5(Hazardous Substances Data)

Usage

Chemical Properties

off-white powder

InChI:InChI=1/C8H7BrO3/c1-12-7-4-5(8(10)11)2-3-6(7)9/h2-4H,1H3,(H,10,11)

Upstream product

• 586-38-9 3-Methoxybenzoic acid 
• 17100-63-9 methyl 4-bromo-3-methoxybenzoate 
• 14348-38-0 4-bromo-3-hydroxybenzoic acid 
• 99-06-9 3-Carboxyphenol 
• 106291-80-9 methyl 4-bromo-3-hydroxybenzoate 
• 50870-42-3 4,4,8,8-Tetrabrom-1-methoxytricyclo<5.1.0.0^3,5>octan 
• 2486-69-3 3-methoxy-4-aminobenzoic acid 
• 43192-34-3 4-bromo-3-methoxybenzaldehyde 
• 50870-44-5 1-(4-bromo-3-methoxyphenyl)ethanone 

Downstream Products

• 149556-41-2 4-bromo-3-methoxybenzoic acid N-isopropyl-N-cyclohexyl amide 
• 17100-64-0 (4-bromo-3-methoxyphenyl)methanol 
• 14348-38-0 4-bromo-3-hydroxybenzoic acid 
• 887757-58-6 2-bromo-5-[(4-methyl-2,3,4,5-tetrahydro-1H-1,5-benzodiazepin-1-yl)carbonyl]phenyl methyl ether 
• 1309682-36-7 4-bromo-N-(2-hydroxyethyl)-3-methoxybenzamide 
• 1309682-37-8 4-bromo-N-(2-hydroxy-2-methylpropyl)-3-methoxybenzamide 
• 1309682-38-9 4-bromo-N-(1-hydroxy-2-methylpropan-2-yl)-3-methoxybenzamide 
• 1309682-39-0 4-bromo-N-(2-ethoxyethyl)-3-methoxybenzamide 
• 1309682-40-3 4-bromo-3-methoxy-N-methyl-N-[2-(methylamino)ethyl]benzamide 
• 1309682-41-4 N-{2-[acetyl(methyl)amino]ethyl}-4-bromo-3-methoxy-N-methylbenzamide 
• 1309682-42-5 tert-butyl {2-[(4-bromo-3-methoxybenzoyl)(methyl)amino]ethyl}methyl-carbamate 
• 1309682-43-6 4-bromo-3-methoxy-N-(2,2,2-trifluoroethyl)benzamide 
• 1309682-44-7 4-bromo-3-methoxy-N-[2-(methylsulfonyl)ethyl]benzamide 
• 1366131-57-8 (3-methoxy-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)(morpholino)methanone 

Relevant articles and documents

TYK2 INHIBITORS AND USES THEREOF

The present invention provides compounds, compositions thereof, and methods of using the same for the inhibition of TYK2, and the treatment of TYK2-mediated disorders.

Bifunctional organocatalysts for the asymmetric synthesis of axially chiral benzamides

Bifunctional organocatalysts bearing amino and urea functional groups in a chiral molecular skeleton were applied to the enantioselective synthesis of axially chiral benzamides via aromatic electrophilic bromination. The results demonstrate the versatilit

METHOD FOR PREPARING SUBSTITUTED TRIAZOLOPYRIDINES

The present invention relates to methods of preparing substituted triazolopyridine compounds of general formula (I) as described and defined herein, as well as to intermediate compounds useful in the preparation of said compounds.