874210-38-5

Basic information

• Product Name: 1,3-Benzenedicarboxylic acid, 4,6-bis[2-[2-(2-methoxyethoxy)ethoxy]ethoxy]-, monomethyl ester
• CAS NO: 874210-38-5
• Molecular Formula: C23H36O12
• Molecular Weight: 504.532
• Mol File: 874210-38-5.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 1,3-Benzenedicarboxylic acid, 4,6-bis[2-[2-(2-methoxyethoxy)ethoxy]ethoxy]-, monomethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: 1,3-Benzenedicarboxylic acid, 4,6-bis[2-[2-(2-methoxyethoxy)ethoxy]ethoxy]-, monomethyl ester(874210-38-5)
• EPA Substance Registry System: 1,3-Benzenedicarboxylic acid, 4,6-bis[2-[2-(2-methoxyethoxy)ethoxy]ethoxy]-, monomethyl ester(874210-38-5)

Safety Data

• Hazardous Substances Data: 874210-38-5(Hazardous Substances Data)

Upstream product

• 19829-74-4 4,6-dihydroxyisophthalic acid 
• 62921-74-8 2-(2-(2-methoxyethoxy)ethoxy)ethyl p-toluenesulfonate 
• 52959-28-1 dimethyl 4,6-dihydroxyisophthalate 
• 874210-29-4 4,6-bis{2-[2-(2-methoxyethoxy)ethoxy]ethoxy}isophthalic acid dimethyl ester 

Downstream Products

• 1239762-33-4 C₂₈H₄₇NO₁₁ 
• 1239762-31-2 C₂₇H₄₅NO₁₁ 
• 936354-38-0 4,6-bis-{2-[2-(2-methoxy-ethoxy)-ethoxy]-ethoxy}-N-(2-tritylsulfanyl-ethyl)-isophthalamic acid 
• 1178882-05-7 C₂₃H₃₅ClO₁₁ 

Relevant articles and documents

Sequence-specific association in aqueous media by integrating hydrogen bonding and dynamic covalent interactions

Oligoamide strands that associate in a sequence-specific fashion into hydrogen-bonded duplexes in nonpolar solvents were converted into disulfide cross-linked duplexes in aqueous media. Thus, by incorporating trityl-protected thiol groups, which allows the reversible formation of disulfide bonds, into the oligoamide strands, only duplexes consisting of complementary hydrogen-bonding sequences were formed in aqueous solution as well as in methanol. The sequence-specific cross-linking of oligoamide strands was confirmed by MALDI-TOF, reverse-phase HPLC, and by isolating a cross-linked duplex. This study demonstrates that the sequence-specificity characteristic of multiply hydrogen-bonded systems can be extended into competitive media through the interplay of H-bonding and reversible covalent interactions, based on which a new class of molecular associating and ligating units that are compatible with both polar and nonpolar environments can be conveniently obtained. Copyright