113585-37-8 Usage
Chemical structure
1,3-Benzenedicarboxylic acid, 5,5'-[[2-(ethoxycarbonyl)-1,3-phenylene]bis(methyleneoxy)]bisis a chemical compound with a benzene ring, two carboxylic acid groups, two 1,3-phenylene groups, methyleneoxy bridges, and ethoxycarbonyl groups.
Plasticizer
Used in the production of various plastic products.
Solvent
Used for cellulose acetate.
Drug delivery
Potential candidate for drug delivery systems due to its biocompatibility and ability to enhance the solubility of poorly soluble drugs.
Reproductive toxicity
Linked to reproductive toxicity in animal studies.
Developmental toxicity
Linked to developmental toxicity in animal studies.
Precaution
It is important to use this compound with caution due to its potential toxic effects.
Check Digit Verification of cas no
The CAS Registry Mumber 113585-37-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,3,5,8 and 5 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 113585-37:
(8*1)+(7*1)+(6*3)+(5*5)+(4*8)+(3*5)+(2*3)+(1*7)=118
118 % 10 = 8
So 113585-37-8 is a valid CAS Registry Number.
113585-37-8Relevant articles and documents
Synthesis, Characterization, and X-ray Structure of the Ruthenium "Picnic-Basket" Porphyrins
Collman, James P.,Brauman, John I.,Fitzgerald, Jeffrey P.,Hampton, Philip D.,Naruta, Yoshinori,et al.
, p. 3477 - 3486 (2007/10/02)
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.
