2531-63-7

Basic information

• Product Name: 2,3-DIMETHOXY-6-NITRO-BENZALDEHYDE
• Synonyms: 2,3-DIMETHOXY-6-NITRO-BENZALDEHYDE;5,6-dimethoxy-2-nitrobenzaldehyde
• CAS NO: 2531-63-7
• Molecular Formula: C₉H₉NO₅
• Molecular Weight: 211.17
• Mol File: 2531-63-7.mol
• Article Data: 13

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2,3-DIMETHOXY-6-NITRO-BENZALDEHYDE(CAS DataBase Reference)
• NIST Chemistry Reference: 2,3-DIMETHOXY-6-NITRO-BENZALDEHYDE(2531-63-7)
• EPA Substance Registry System: 2,3-DIMETHOXY-6-NITRO-BENZALDEHYDE(2531-63-7)

Safety Data

• Hazardous Substances Data: 2531-63-7(Hazardous Substances Data)

Usage

General Description

2,3-DIMETHOXY-6-NITRO-BENZALDEHYDE is a chemical compound with the molecular formula C9H9NO5. It is a yellow crystalline solid that is commonly used as an intermediate in the synthesis of pharmaceuticals and agrochemicals. 2,3-DIMETHOXY-6-NITRO-BENZALDEHYDE is known for its aromatic and aldehyde properties, making it useful in organic synthesis. It is also used as a reagent in various chemical reactions, including the synthesis of 2,4-Dimethoxyphenethylamine. However, it is important to handle this chemical with care as it is known to be harmful if inhaled or ingested, and can cause irritation to the skin and eyes upon contact.

Upstream product

• 2426-86-0 2-hydroxy-3-methoxy-6-nitrobenzaldehyde 
• 77-78-1 dimethyl sulfate 
• 86-51-1 2,3-dimethyoxybenzaldehyde 
• 7697-37-2 nitric acid 
• 64-19-7 acetic acid 
• 24677-78-9 2,3-dihydroxybenzaldehyde 
• 103483-19-8 2-Hydroxy-3-methoxy-6-nitrobenzaldehyde potassium salt 
• 2426-60-0 2-Hydroxy-3-methoxy-6-nitrobenzaldehyde benzenesulfonate 
• 2426-85-9 2-Hydroxy-3-methoxybenzaldehyde benzenesulfonate 
• 111042-36-5 2-Hydroxy-3-methoxy-6-nitrobenzaldehyde, sodium salt 
• 74-88-4 methyl iodide 
• 7461-60-1 2,3-dimethoxycinnamic acid 
• 148-53-8 3-methoxy-2-hydroxybenzaldehyde 

Downstream Products

• 92210-37-2 2,3-Dimethoxy-6-nitrobenzaldehyde ethylene acetal 
• 2426-86-0 2-hydroxy-3-methoxy-6-nitrobenzaldehyde 
• 1027150-95-3 (2,3-dimethoxy-6-nitro-phenyl)-(3,4,5-trimethoxy-phenyl)-methanol 
• 99055-59-1 methyl 2-nitro-5,6-dimethoxybenzoate 
• 858238-93-4 2-phenyl-quinoline-5,6-diol 
• 860717-33-5 5,6-dimethoxy-2-phenyl-quinoline-3-carbonitrile 
• 412337-46-3 (5,6-dimethoxy-2-methyl-[3]quinolyl)-phenyl ketone 
• 860205-34-1 5,6-dimethoxy-2-phenyl-quinoline-3-carboxylic acid 
• 72517-26-1 2,3-dimethoxy-6-nitrobenzoic acid 
• 30933-67-6 4,5-dimethoxy-1H-indole 
• 1269920-19-5 4-[1-(4-fluorobenzyl)-4,5-dimethoxy-1H-indol-3-yl]-2-hydroxy-4-oxobut-2-enoic acid 
• 1269920-14-0 ethyl 4-[1-(4-fluorobenzyl)-4,5-dimethoxy-1H-indol-3-yl]-2-hydroxy-4-oxobut-2-enoate 
• 1269920-09-3 3-acetyl-4,5-dimethoxy-1-(4-fluorobenzyl)-1H-indole 
• 90916-24-8 2,3-dimethoxy-6,β-dinitrostyrene 

Relevant articles and documents

3-INDOLYL FURANOIDS AS INHIBITORS OF MATRIX METALLOPROTEINASE-9 FOR PREVENTION OF GASTRIC ULCER AND OTHER INFLAMMATORY DISEASES

Disclosed are 3-indolyl furanoid compounds which are useful as potent anti-inflammatory agents and prevent gastric ulcer by inhibiting matrix metalloproteinase-9 (MMP-9) expression in gastric mucosal layer. For example, disclosed is a compound of formula 1, wherein: R1 to R6 is selected from H, OH, CH3, OCH3, Br, Cl, Ph or o-OHC6H4, OCH2—CH═CH2, or OCH2CH2CH3, and R1 to R6 is having at least one substituent with alkyl, aryl and heteroaryl groups other than H, wherein the carbon in alkyl, aryl and heteroaryl is in the range of C1 to C8. Various embodiments relate to representative compounds of Formula 1 and method of preparation thereof. Further embodiments relates to the use of representative compounds of Formula 1 in treating diseases associated with gastric ulcer and other inflammatory diseases. A noted feature of an embodiment is the IC50 value of 50 μM of one of the 3-indolyl furanoids.

Synthesis and adrenolytic activity of new propanolamines

The synthesis of (2R, S)-1-(6-methoxy-4-(methoxymethyl)-1H-indol-5-yloxy)- 3-(2-(2-methoxyphenoxy)ethylamino)propan-2-ol and (2R, S)-1-(4-methoxy-6- (methoxymethyl)-1H-indol-5-yloxy)-3-(2-(2-methoxyphenoxy)ethylamino)propan-2-ol is described. The compound

NEW DS DNA BINDING FLUORESCENT DYES

The present invention is directed to a fluorescent dye comprising a benzothiazolium moiety and a pyrimidinium moiety connected by a mono-methine bridge, characterized in that (i) the 2-position of the pyrimidine carries a substituent which starts with a C