7507-86-0

Basic information

• Product Name: 2-Bromo-5-methoxybenzaldehyde
• Synonyms: 2-BROMO-5-METHOXYBENZALDEHYDE;AKOS B004279;2-BROMO-4-METHOXYBENZALDEHYDE;3-Methoxy-6-bromobenzaldehyde;4-Bromo-3-formylanisole;4-Bromo-3-formylanisole, 6-Bromo-m-anisaldehyde;2-Bromo-5-methoxybenzaldehyde 97%;EOS-60499
• CAS NO: 7507-86-0
• Molecular Formula: C₈H₇BrO₂
• Molecular Weight: 215.04
• Product Categories: Aromatic Aldehydes & Derivatives (substituted);Benzaldehyde;Aryl;Halogenated;Organohalides;Adehydes, Acetals & Ketones;Anisoles, Alkyloxy Compounds & Phenylacetates;Bromine Compounds;aldehyde| alkyl bromide
• Mol File: 7507-86-0.mol
• Article Data: 68

Chemical Properties

• Melting Point: 71-76 ºC
• Boiling Point: 284.3 °C at 760 mmHg
• Flash Point: 125.7 °C
• Appearance: /
• Density: 1.522 g/cm³
• Vapor Pressure: 0.003mmHg at 25°C
• Refractive Index: 1.585
• Storage Temp.: Room temperature.
• Solubility: Acetonitrile (Slightly), Chloroform (Slightly)
• CAS DataBase Reference: 2-Bromo-5-methoxybenzaldehyde(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Bromo-5-methoxybenzaldehyde(7507-86-0)
• EPA Substance Registry System: 2-Bromo-5-methoxybenzaldehyde(7507-86-0)

Safety Data

• Hazard Codes: Xi,Xn
• Statements: 36/37/38-22
• Safety Statements: 26-36/37/39
• WGK Germany: 3
• HazardClass: IRRITANT
• Hazardous Substances Data: 7507-86-0(Hazardous Substances Data)

Usage

Chemical Properties

White powder

Uses

2-Bromo-5-methoxybenzaldehyde is used in preparation of Benzimidazole Quinolines. Also, used in preparation of Cyclopentenes, Polycycles, Benzocarbocycles/N-Heterocycle derivatives.

InChI:InChI=1/C8H7BrO2/c1-11-7-3-2-6(5-10)8(9)4-7/h2-5H,1H3

Upstream product

• 591-31-1 3-methoxy-benzaldehyde 
• 2973-80-0 2-bromo-5-hydroxybenzaldehyde 
• 74-88-4 methyl iodide 
• 6971-51-3 3-methoxybenzyl alcohol 
• 150192-39-5 2-Bromo-5-methoxybenzyl alcohol 
• 77-78-1 dimethyl sulfate 
• 681427-75-8 1-bromo-2-dibromomethyl-4-methoxybenzene 
• 22921-68-2 2-bromo-5-methoxy-benzoic acid 
• 27060-75-9 4-bromo-3-methylanisole 
• 19614-12-1 2-bromo-5-methoxybenzyl bromide 
• 100-83-4 meta-hydroxybenzaldehyde 
• 20357-24-8 5-methoxy-2-nitro-benzaldehyde 
• 26831-52-7 2-amino-5-methoxybenzaldehyde 
• 1171119-65-5 5-(2-bromo-5-methoxybenzylidene)-2,2-dimethyl-1,3-dioxane-4,6-dion 

Downstream Products

• 881650-52-8 2-bromo-5-methoxy-trans-cinnamic acid 
• 110051-14-4 3t-(2-bromo-5-methoxy-phenyl)-1-(1-hydroxy-4-nitro-[2]naphthyl)-propenone 
• 150192-39-5 2-Bromo-5-methoxybenzyl alcohol 
• 22921-68-2 2-bromo-5-methoxy-benzoic acid 
• 133609-38-8 (2-Brom-5-methoxybenzoyl-)essigsaeureethylester 
• 105728-91-4 5,10,15,20-tetrakis(2-bromo-5-methoxyphenyl)porphyrin 
• 100516-29-8 9-(2-bromo-5-methoxybenzylidene)fluorene 
• 105479-90-1 5-methoxy-2-(methylthio)benzaldehyde 
• 83986-17-8 2-(2-Flurophenylthio)-5-methoxybenzaldehyde 
• 115046-51-0 2-[1-(2-Bromo-5-methoxy-phenyl)-meth-(E)-ylidene]-succinic acid 4-tert-butyl ester 1-methyl ester 
• 133966-27-5 2,7-Bis-[(E)-2-(2-bromo-5-methoxy-phenyl)-vinyl]-naphthalene 
• 84884-56-0 2-(2,5-difluorophenylthio)-5-hydroxybenzaldehyde 
• 83975-63-7 2-(2,5-Difluorophenylthio)-5-methoxybenzaldehyde 
• 98015-07-7 2-Bromo-5-methoxybenzaldehyde ethylene glycol acetal 

Relevant articles and documents

Elaboration of the isochromane system of stephaoxocanes employing an Oxa-Pictet Spengler type cyclization

An approach to the synthesis of the isochromane moiety embodying the AC-ring system of the stephaoxocanes, by the use of an Oxa-Pictet Spengler type cyclization strategy, is reported.

COMPOUNDS AND COMPOSITIONS FOR USE IN TREATING SKIN DISORDERS

Provided herein is a compound of formula (XXXII) or a pharmaceutically acceptable salt, solvate, hydrate, stereoisomer thereof or a physiologically functional derivative thereof, wherein R1, R2, R3, G, A, E, n, p, and q are defined herein. Also provided herein are compositions comprising a compound of formula (XXXII), and methods of using a compound of formula (XXXII), e.g., in the treatment or prevention of skin disorders.

Atroposelective Total Synthesis of the Fourfold ortho-Substituted Naphthyltetrahydroisoquinoline Biaryl O,N-Dimethylhamatine

A stereoselective total synthesis of O,N-dimethylhamatine, an analogue of an axially chiral naphthylisoquinoline natural biaryl product from tropical Ancistrocladus lianas, is reported. The route features a late-stage atropo-diastereoselective biaryl bond