738616-33-6

Basic information

• Product Name: 2-[bis(3,4-dimethoxyphenyl)methyl]-5,6-dimethoxy-2-methyl-1H-indene-1,3(2H)-dione
• Synonyms: 2-[bis(3,4-dimethoxyphenyl)methyl]-5,6-dimethoxy-2-methyl-1H-indene-1,3(2H)-dione
• CAS NO: 738616-33-6
• Molecular Weight: 506.552
• Mol File: 738616-33-6.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 2-[bis(3,4-dimethoxyphenyl)methyl]-5,6-dimethoxy-2-methyl-1H-indene-1,3(2H)-dione(CAS DataBase Reference)
• NIST Chemistry Reference: 2-[bis(3,4-dimethoxyphenyl)methyl]-5,6-dimethoxy-2-methyl-1H-indene-1,3(2H)-dione(738616-33-6)
• EPA Substance Registry System: 2-[bis(3,4-dimethoxyphenyl)methyl]-5,6-dimethoxy-2-methyl-1H-indene-1,3(2H)-dione(738616-33-6)

Safety Data

• Hazardous Substances Data: 738616-33-6(Hazardous Substances Data)

Upstream product

• 74084-26-7 3,3',4,4'-tetramethoxybenzhydrole 
• 738616-34-7 5,6-dimethoxy-2-methyl-1H-indene-1,3(2H)-dione 
• 74-88-4 methyl iodide 
• 738616-29-0 2-[bis(3,4-dimethoxyphenyl)methyl]-5,6-dimethoxy-1H-indene-1,3(2H)-dione 
• 2107-69-9 5,6-dimethoxy-1-indanone 
• 91-16-7 1,2-dimethoxybenzene 
• 531-88-4 5,6-dimethoxyphthalide 
• 36517-91-6 2,3-dihydro-5,6-dimethoxy-1H-indene-1,3-dione 
• 4131-03-7 bis(3,4-dimethoxyphenyl)methanone 
• 40125-46-0 3-BROMO-5,6-DIMETHOXY-PHTHALIDE 
• 93-07-2 Veratric acid 
• 738616-38-1 3-[(E)-ethylidene]-5,6-dimethoxy-2-benzofuran-1(3H)-one 
• 2859-78-1 4-Bromoveratrole 
• 120-14-9 3,4-dimethoxy-benzaldehyde 

Downstream Products

• 738616-39-2 all-cis-2-[bis(3,4-dimethoxyphenyl)methyl]-5,6-dimethoxy-2-methyl-1,3-indanediol 

Relevant articles and documents

Dynamic Transformation between Covalent Organic Frameworks and Discrete Organic Cages

We propose a dynamic covalent chemistry (DCC)-induced linker exchange strategy for the structural transformation between covalent organic frameworks (COFs) and cages for the first time. Studies have shown that the COF-to-cage and cage-to-COF transformatio

Rigidification of a macrocyclic tris-catecholate scaffold leads to electronic localisation of its mixed valent redox product

The catecholate groups in [{Pt(L)}3(μ3-tctq)] (H6tctq = 2,3,6,7,10,11-hexahydroxy-4b,8b,12b,12d-tetramethyltribenzotriquinacene; L = a diphosphine chelate) undergo sequential oxidation to their semiquinonate forms by voltammetry, with ΔE1/2 = 160-170 mV. The monoradical [{Pt(dppb)}3(μ3-tctq)]+ is valence-localised, with no evidence for intervalence charge transfer in its near-IR spectrum. This contrasts with previously reported [{Pt(dppb)}3(μ3-ctc)]+ (H6ctc = cyclotricatechylene), based on the same macrocyclic tris-dioxolene scaffold, which exhibits partly delocalised (class II) mixed valency.