874758-53-9 Usage
Chemical structure
A complex organic molecule with a benzodioxole ring, an acetic acid group, and additional functional groups such as hydroxy, methoxymethoxy, and ethyl ester.
Molecular weight
Approximately 332 g/mol (calculated from the molecular formula)
Benzodioxole ring
A fused ring system consisting of a benzene ring and a dioxole (oxygen-containing) ring.
Acetic acid group
A carboxylic acid functional group (-COOH) attached to a methyl group.
Hydroxy groups
Two hydroxyl (-OH) groups present in the molecule.
Methoxymethoxy group
A methoxy (-OCH3) group connected to a methoxymethoxy (-OCH2O-) group.
Ethyl ester group
An ester formed by the reaction of the carboxylic acid group with an alcohol (ethanol), resulting in an ethyl ester (-COOEt) group.
Potential pharmaceutical applications
As an anti-inflammatory and analgesic agent, it may be used in the development of new drugs for the treatment of various inflammatory and pain-related conditions.
Bioavailability and pharmacokinetic properties
The addition of the ethyl ester group may enhance the compound's bioavailability, which refers to the extent and rate at which the drug is absorbed and becomes available to the target site in the body.
Interactions with biological systems
The presence of hydroxy and methoxymethoxy groups in the molecule suggests potential interactions with biological systems, which may contribute to its therapeutic effects.
Further research
More research is needed to fully understand the therapeutic potential of this chemical compound and its applications in the development of new drugs.
Solubility
The solubility of 1,3-Benzodioxole-4-acetic acid, α,7-dihydroxy-6-(methoxymethoxy)-, ethyl ester is not provided in the material, but it can be inferred that it may be soluble in organic solvents such as ethanol, methanol, or dimethyl sulfoxide (DMSO) due to the presence of the ethyl ester and methoxymethoxy groups.
Stability
The stability of 1,3-Benzodioxole-4-acetic acid, α,7-dihydroxy-6-(methoxymethoxy)-, ethyl ester is not mentioned in the material, but it is generally expected that such organic molecules may be sensitive to light, heat, and moisture, and should be stored under appropriate conditions to maintain their integrity.
Check Digit Verification of cas no
The CAS Registry Mumber 874758-53-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,4,7,5 and 8 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 874758-53:
(8*8)+(7*7)+(6*4)+(5*7)+(4*5)+(3*8)+(2*5)+(1*3)=229
229 % 10 = 9
So 874758-53-9 is a valid CAS Registry Number.
874758-53-9Relevant academic research and scientific papers
Combination of lithium chloride and hexafluoroisopropanol for friedel-crafts reactions
Willot, Matthieu,Chen, JinChun,Zhu, Jieping
experimental part, p. 577 - 580 (2009/07/01)
A combination of weak Lewis acid (LiCl) and weak Br?nsted acid (hexafluoroisopropanol, HFIP) promotes efficiently the Friedel-Crafts reaction of electron-rich aromatic compounds with ethyl glyoxylate. Georg Thieme Verlag Stuttgart.
Intermediate and process of preparation of ecteinascidin using such intermediate
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Page/Page column 17; 22-23, (2008/06/13)
The present invention concerns an intermediate of the following formula I in which R1 and R2 represent independently of each other a C1-C12 alkyl group, a (C1-C12 alkoxy)carbonyl group, opt
Total synthesis of ecteinascidin 743
Chen, Jinchun,Chen, Xiaochuan,Bois-Choussy, Michele,Zhu, Jieping
, p. 87 - 89 (2007/10/03)
A convergent total synthesis of ecteinascidin 743 is realized from five building blocks of almost equal size. It takes 23 steps from l-3-hydroxy-4-methoxy-5-methyl phenylalanol (5) with an overall yield of 3%. Copyright
