113585-41-4

Basic information

• Product Name: 1,3-Benzenedicarbonyl dichloride, 5,5'-[1,4-phenylenebis(methyleneoxy)]bis-
• CAS NO: 113585-41-4
• Molecular Formula: C24H14Cl4O6
• Molecular Weight: 540.184
• Mol File: 113585-41-4.mol

Chemical Properties

• CAS DataBase Reference: 1,3-Benzenedicarbonyl dichloride, 5,5'-[1,4-phenylenebis(methyleneoxy)]bis-(CAS DataBase Reference)
• NIST Chemistry Reference: 1,3-Benzenedicarbonyl dichloride, 5,5'-[1,4-phenylenebis(methyleneoxy)]bis-(113585-41-4)
• EPA Substance Registry System: 1,3-Benzenedicarbonyl dichloride, 5,5'-[1,4-phenylenebis(methyleneoxy)]bis-(113585-41-4)

Safety Data

• Hazardous Substances Data: 113585-41-4(Hazardous Substances Data)

Upstream product

• 113585-33-4 C₃₂H₃₄O₁₀ 
• 39630-68-7 diethyl 5-hydroxyisophthalate 
• 618-83-7 5-Hydroxyisophthalic acid 
• 22937-66-2 5,5′-(1,4-phenylenebis(methylene))bis(oxy)diisophthalate 
• 13036-02-7 Dimethyl 5-hydroxyisophthalate 
• 623-24-5 1,4-bis(bromomethyl)benzene 
• 22937-70-8 5,5′-phenylenebis(methylene)-1,1′-3,3′-(benzene-tetracarboxylic acid) 

Relevant articles and documents

Dendrimers with alternating amine and ether generations

Dendrimers having alternating aryl benzyl ether and tertiary amine generations and up to 16 bis-(2-methoxyethyl)amine end groups and four internal tertiary amines were synthesized by sequential etherification, amidation of secondary amines, and LiAlH

Synthesis, Characterization, and X-ray Structure of the Ruthenium "Picnic-Basket" Porphyrins

The synthesis and characterization of a new class of sterically protected porphyrins, the "picnic-basket" porphyrins, are presented.These tetraarylporphyrins, which were prepared as cytochrome P-450 active-site analogues, bear a rigid superstucture on one face of the porphyrin macrocycle.The cavity defined by the appended superstructure may be readily varied in size, chirality, and functionality.In addition, the synthesis and characterization, including an X-ray structure, of several ruthenium picnic-basket porphyrin carbonyl complexes are reported.The regiochemistry of axial ligation in these ruthenium derivatives has been determined by 1H NMR spectroscopy.