75956-64-8

Basic information

• Product Name: 2,3-Dimethoxy-4-(methoxycarbonyl)benzoylchlorid
• Synonyms: 2,3-Dimethoxy-4-(methoxycarbonyl)benzoylchlorid
• CAS NO: 75956-64-8
• Molecular Weight: 258.658
• Mol File: 75956-64-8.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: 2,3-Dimethoxy-4-(methoxycarbonyl)benzoylchlorid(CAS DataBase Reference)
• NIST Chemistry Reference: 2,3-Dimethoxy-4-(methoxycarbonyl)benzoylchlorid(75956-64-8)
• EPA Substance Registry System: 2,3-Dimethoxy-4-(methoxycarbonyl)benzoylchlorid(75956-64-8)

Safety Data

• Hazardous Substances Data: 75956-64-8(Hazardous Substances Data)

Upstream product

• 75956-63-7 sodium methyl 2,3-dimethoxyterephthalate 
• 7168-94-7 dimethyl 2,3-dimethoxyterephthalate 

Downstream Products

• 75956-66-0 N,N',N'',N'''-tris<2,3-dimethoxy-4-(carbomethoxy)benzoyl>-1,5,10-triazadecane 
• 131933-29-4 C₃₉H₄₈N₄O₁₅ 
• 110354-51-3 C₃₉H₄₅Cl₃N₄O₁₂ 
• 131973-28-9 C₄₂H₅₄N₄O₁₅ 
• 75956-65-9 N,N',N'',N'''-tetrakis<2,3-dimethoxy-4-(carbomethoxy)benzoyl>-1,5,10,14-tetraazatetradecane 
• 128262-57-7 2,3-Dimethoxy-N,N-ditetradecyl-terephthalamic acid methyl ester 
• 153502-64-8 methyl-2,3-dimethoxy-4-(methylcarbamoyl)benzoate 
• 114370-80-8 C₅₄H₆₈N₆O₂₀ 
• 1160934-36-0 C₃₈H₄₆N₄O₁₄ 
• 1112984-92-5 C₃₈H₄₈N₂O₁₂ 
• 75956-67-1 N,N',N'',N'''-tetrakis(2,3-dihydroxy-4-carboxybenzoyl)-1,5,10,14-tetraazatetradecane 
• 75956-68-2 N,N',N'',N'''-tris(2,3-dihydroxy-4-carboxybenzoyl)-1,5,10-triazadecane 
• 145731-74-4 C₃₇H₃₆Cl₂N₂O₈ 
• 772306-42-0 C₃₆H₄₂N₄O₁₅ 

Relevant articles and documents

Chiral amide directed assembly of a diastereo- and enantiopure supramolecular host and its application to enantioselective catalysis of neutral substrates

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Gallium(III) catecholate complexes as probes for the kinetics and mechanism of inversion and isomerization of siderophore complexes

The catechol siderophore analog K3[Ga(3)3], 4 (H23 = 2,3-dihydroxy-N,N'-diisopropylterephthalamide), is D3-symmetric in aqueous solution, and exists in two enantiomeric forms, Δ-4 and Λ-4. Variable temperature N

Azaparacyclophanes with Metal-binding Sites. Part 1. Preparation, Characterization, and Molecular Recognition Behaviour of Hexapus Azaparacyclophane and its Iron(III) Complex

All the catechol moieties of a hexapus triazaparacyclophane having three catechol moieties and six hydrocarbon chains (1) undergo coordination interactions with the iron(III) ion in a 1:1 molar ratio of 1 to iron(III) above pH 6 in an aqueous medium.Two different iron(III) complexes of 1, A and B in a 1:1 molar ratio, are in the high spin iron(III) state as characterized by electronic, EPR and Moessbauer spectroscopy: A is a hexacoordinated mononulear complex with half-protonated catecholato groups, subjected to considerable structural distortion; B is ahexacoordinated mononuclear complex with complete dissociation of all the catechol protons, retaining high structural symmetry.The molecular recognition behaviour of 1 and Fe-complex A toward hydrophobic guest molecules has been investigated in aqueous HEPES and acetate buffers at 30.0 deg C and μ 0.10 mol dm-3.The hexapus cyclophane 1 recognizes organic guests through hydrophobic and electrostatic interactions; anionic and non-ionic quests, 7-hydroxy-8-phenylazonaphthalene-1,3-disulfonate (OG) and 2-hydroxy-1-(2-pyridylazo)naphthalene (PAN), respectively, are incorporated into host 1 with binding constants of the order of 105 dm3 mol-1, while a cationic guest, 2-(p-dimethylaminostyryl)-1-ethylquinolinium (QR), is not included in the host.The guest-binding behaviour of Fe-complex A toward OG and PAN is much enhanced relative to that of 1 as effected by hydrophobic, electrostatic and coordination interactions under conditions identical to those applied to 1; the binding constant for OG is nearly pH-independent in a pH range of 3-8, while that for PAN is pH-dependent because the coordination interaction with the host is subject to change by pH.