81574-75-6

Basic information

• Product Name: Methyl 2,4-dimethoxy-5-nitrobenzoate
• Synonyms: Methyl 2,4-dimethoxy-5-nitrobenzoate;2,4-Dimethoxy-5-nitro-benzoic acid methyl ester
• CAS NO: 81574-75-6
• Molecular Formula: C₁₀H₁₁NO₆
• Molecular Weight: 241.19744
• Mol File: 81574-75-6.mol
• Article Data: 6

Chemical Properties

• Appearance: /
• Storage Temp.: 2-8°C
• CAS DataBase Reference: Methyl 2,4-dimethoxy-5-nitrobenzoate(CAS DataBase Reference)
• NIST Chemistry Reference: Methyl 2,4-dimethoxy-5-nitrobenzoate(81574-75-6)
• EPA Substance Registry System: Methyl 2,4-dimethoxy-5-nitrobenzoate(81574-75-6)

Safety Data

• Hazardous Substances Data: 81574-75-6(Hazardous Substances Data)

Upstream product

• 101495-62-9 methyl 2,4-dichloro-5-nitrobenzoate 
• 124-41-4 sodium methylate 
• 89-86-1 4-hydroxysalicylic acid 
• 90564-41-3 2,4-dimethoxy-5-nitrobenzoic acid 
• 19861-62-2 2,4-dichloro-5-nitrobenzoic acid 
• 115919-39-6 2-methoxy-4,5-dinitrobenzoic acid 
• 2597-56-0 4-nitro-o-anisic acid 
• 13120-77-9 2-methyl-5-nitroanisole 
• 58137-79-4 methyl 6-bromo-2,4-dimethoxybenzoate 
• 81574-69-8 2-bromo-4,6-dimethoxybenzaldehyde 
• 20469-65-2 1-bromo-3,5-dimethoxybenzene 
• 13722-96-8 2,4-dihydroxy-5-nitrobenzoic acid 
• 271261-71-3 2,4-dihydroxy-5-nitro-benzoic acid methyl ester 
• 77-78-1 dimethyl sulfate 

Downstream Products

• 271261-78-0 3-(5-(2,4-dimethoxy-5-nitrobenzoylamino)-2,4-dioctyloxybenzoylamino)-4-methoxytoluene 
• 874210-60-3 C₅₃H₇₂N₄O₂₁ 
• 827325-32-6 C₅₃H₇₄N₄O₁₉ 
• 874210-72-7 4-(4-(2,4-dimethoxy-5-nitro-benzoylamino)-5-(3-ethoxycarbonyl-propoxy)-2-{5-[2-(3-ethoxycarbonyl-propoxy)-5-methyl-phenylcarbamoyl]-2,4-dimethoxy-phenylcarbamoyl}-phenoxy)-butyric acid ethyl ester 
• 874210-59-0 C₄₄H₆₃N₃O₁₈ 
• 827325-31-5 C₄₄H₆₅N₃O₁₆ 

Relevant articles and documents

Multiturn Hollow Helices: Synthesis and Folding of Long Aromatic Oligoamides

Aromatic oligoamides adopting helical conformations are synthesized by coupling carboxyl-terminated basic units having two, four, and eight residues to amine-terminated oligomer precursors. Coupling yields show no noticeable reduction with the size of the

A new class of folding oligomers: Crescent oligoamides [4]

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Cerium(IV)-induced nitration of cinnamic acids. Novel remote electrophilic substitution

The treatment of (E)-3,4-dimethoxycinnamic acid with ceric amonium nitrate in trifluoroacetic acid afforded (E)1,2-dimethoxy-4-nitro-5-(2-nitroethenyl)benzene in 79percent yield.The unusual ipso substitution of the carboxylic acid moiety by a nitro functional center illustrated a new reaction manifold of cerium(IV).Six cinnamic acids were examined to ascertain the generality of the transformation.The bidentate nitrato structure of the metal salt is believed to account for the nitrating ability of this system.