192810-12-1

Basic information

• Product Name: METHYL 5-BROMO-3-HYDROXYBENZOATE
• Synonyms: METHYL 5-BROMO-3-HYDROXYBENZOATE;3-BROMO-5-HYDROXY-BENZOIC ACID METHYL ESTER;BENZOIC ACID, 3-BROMO-5-HYDROXY-, METHYL ESTER
• CAS NO: 192810-12-1
• Molecular Formula: C₈H₇BrO₃
• Molecular Weight: 231.044
• Product Categories: Aromatic Esters
• Mol File: 192810-12-1.mol
• Article Data: 21

Chemical Properties

• Melting Point: 130-135℃
• Boiling Point: 331.251 °C at 760 mmHg
• Flash Point: 154.135 °C
• Appearance: /
• Density: 1.628 g/cm³
• Storage Temp.: Sealed in dry,Room Temperature
• PKA: 8.19±0.10(Predicted)
• Water Solubility: Slightly soluble in water.
• CAS DataBase Reference: METHYL 5-BROMO-3-HYDROXYBENZOATE(CAS DataBase Reference)
• NIST Chemistry Reference: METHYL 5-BROMO-3-HYDROXYBENZOATE(192810-12-1)
• EPA Substance Registry System: METHYL 5-BROMO-3-HYDROXYBENZOATE(192810-12-1)

Safety Data

• Hazardous Substances Data: 192810-12-1(Hazardous Substances Data)

Usage

Uses

It is employed as intermediate for pharmaceutical.

Upstream product

• 1025718-78-8 methyl 3-bromo-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzoate 
• 51329-15-8 methyl 3,5-dibromobenzoate 
• 67-56-1 methanol 
• 140472-69-1 3-bromo-5-hydroxy-benzoic acid 
• 618-95-1 methyl 3-nitrobenzoate 
• 706791-83-5 3-amino-5-bromobenzoic acid methyl ester 
• 75-36-5 acetyl chloride 

Downstream Products

• 905917-51-3 3-(2-aminopyrimidin-4-yl)-5-bromophenol 
• 1186519-88-9 methyl 3-hydroxy-5-(5-methylpyridin-2-yl)benzoate 
• 1307254-88-1 C₂₀H₂₆BrNO₅ 
• 1310808-01-5 5-[3-bromo-5-(methoxycarbonyl)phenoxy]pyrazine-2-carboxylic acid 
• 1310809-49-4 C₁₇H₁₇BrN₂O₅ 
• 1430229-98-3 C₂₁H₁₅BrClN₃O₄ 
• 1004294-79-4 methyl 3-hydroxy-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzoate 
• 1605326-32-6 (S)-3-(4-amino-6-((1-(5-methyl-4-oxo-3-phenyl-3,4-dihydropyrrolo[2,1-f][1,2,4]triazin-2-yl)ethyl)amino)pyrimidin-5-yl)-5-hydroxybenzoic acid 
• 1605328-63-9 (S)-methyl 3-(4-amino-6-((1-(5-methyl-4-oxo-3-phenyl-3,4-dihydropyrrolo[2,1-f][1,2,4]triazin-2-yl)ethyl)amino)pyrimidin-5-yl)-5-hydroxybenzoate 

Relevant articles and documents

Enantioselectivity Induced by Stereoselective Interlocking: A Novel Core Motif for Tropos Ligands

Well-defined supramolecular interactions are a powerful tool to control the stereochemistry of a catalytic reaction. In this paper, we report a novel core motif for fluxional 2,2′-biphenyl ligands carrying (S)-amino acid-derived interaction sites in 5,5′-

NOVEL HETEROARYL-TRIAZOLE COMPOUNDS AS PESTICIDES

The present invention relates to novel heteroaryl-triazole and heteroaryl-tetrazole compounds of the general formula (I), in which the structural elements R1, R2, R3, R4 and R5 have the meaning given in the description, to formulations and compositions comprising such compounds and for their use in the control of animal pests including arthropods and insects in plant protection and to their use for control of ectoparasites on animals.

NOVEL HETEROARYL-TRIAZOLE COMPOUNDS AS PESTICIDES

The present invention relates to novel heteroaryl-triazole compounds of the general formula (I), in which the structural elements X, R1, R2, R3 and R4 have the meaning given in the description, to formulations and compositions comprising such compounds and for their use in the control of animal pests including arthropods and insects in plant protection and to their use for control of ectoparasites on animals.