101913-37-5

Basic information

• Product Name: Benzaldehyde, 4,4'-[1,3-propanediylbis(oxy)]bis[3-methoxy-
• Synonyms: 3,3'-Dimethoxy-4,4'-propandiyldioxy-di-benzaldehyd;3,3'-dimethoxy-4,4'-propanediyldioxy-di-benzaldehyde;1,3-bis(4-formyl-2-methoxyphenoxy)propane;Benzaldehyde,4,4'-[1,3-propanediylbis(oxy)]bis[3-methoxy
• CAS NO: 101913-37-5
• Molecular Formula: C19H20O6
• Molecular Weight: 344.364
• Mol File: 101913-37-5.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: Benzaldehyde, 4,4'-[1,3-propanediylbis(oxy)]bis[3-methoxy-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzaldehyde, 4,4'-[1,3-propanediylbis(oxy)]bis[3-methoxy-(101913-37-5)
• EPA Substance Registry System: Benzaldehyde, 4,4'-[1,3-propanediylbis(oxy)]bis[3-methoxy-(101913-37-5)

Safety Data

• Hazardous Substances Data: 101913-37-5(Hazardous Substances Data)

Upstream product

• 121-33-5 vanillin 
• 109-64-8 1,3-dibromo-propane 

Downstream Products

• 110316-12-6 1,3-bis<4-(hydroxymethyl)-2-methoxyphenoxy>propane 
• 1224597-74-3 C₄₃H₅₄N₂O₁₂ 
• 1315248-02-2 ethyl 4-[4-(3-(4-[5-(ethoxycarbonyl)-6-methyl-2-thioxo-1,2,3,4-tetrahydro-4-pyrimidinyl]-2-methoxyphenoxy)propoxy)-3-methoxyphenyl]-6-methyl-2-thioxo-1,2,3,4-tetrahydro-5-pyrimidinecarboxylate 
• 1315248-06-6 C₄₁H₅₀N₆O₁₀S₂ 

Relevant articles and documents

Synthesis and characterizations of flexible furfural based molecular receptor for selective recognition of Dy(III) ions

Herein we report the development of a Dy(III) ion specific flexible molecular receptor incorporated with furan group. The capture experiment of several metal ions covering mono, di and trivalent metal ions with synthesized three molecules has been perform

1st generation dendrimeric antioxidants containing Meldrum's acid moieties as surface groups

Free radical-caused oxidative stress can be reduced by various antioxidants. A new and promising type of antioxidant are monosubstituted Meldrum's acids. Herein the first dendritic architecture with 1,3-dioxane-4,6-dione units as surface groups is presented. The compounds were synthesized through the alkylation of phenol, the Knoevenagel condensation and sequential reduction. The antiradical activity (AA) against 1,1-diphenyl-2-picryl hydrazyl (DPPH) for all compounds is 80-90%, and the IC50 varies from 10-35 μM. These data are comparable with vitamin C, t-butylhydroquinone (TBHQ) or vitamin E. The AA against galvinoxyl (GO) increased with the number of surface groups. The AA was comparable with butylated hydroxytoluene (BHT) for compounds with at least two moieties of 1,3-dioxane-4,6-dione. The structure with a flexible glycerol core is highlighted among all the derivatives. Although the AA against DPPH for the glycerol derivative is comparable with those with aromatic cores it is more effective against GO (AA = 95%, IC50 = 60 μM): the AA is greater than for vitamin C and BHT. Thus, a flexible structure seems to be a promising core for elaborating powerful antioxidants with Meldrum's acid surface groups. This journal is

Synthesis and biological evaluation of conformationally flexible as well as restricted dimers of monastrol and related dihydropyrimidones

A series of conformationally flexible and restricted dimers of monastrol as well as related dihydropyrimidones have been synthesized by employing one-pot Biginelli multicomponent reaction. These dimers have been evaluated for cytotoxic potency against sel