873378-07-5 Usage
Explanation
The molecular formula represents the number of atoms of each element present in a molecule of the compound.
Explanation
Benzodioxans are a class of organic compounds that consist of a benzene ring fused to a 1,4-dioxane.
Explanation
Syringic acid is an alternative name for 1,4-Benzodioxan-5-carboxylic acid, 6-hydroxy(4CI), which is derived from its chemical structure.
Explanation
Syringic acid can be found in various plant sources, which may contribute to their antioxidant properties.
5. Antioxidant properties
Explanation
Syringic acid has been shown to possess antioxidant properties, which can help protect cells from damage caused by free radicals.
Explanation
Syringic acid has been studied for its potential health benefits, including its ability to reduce inflammation and inhibit the growth of certain microorganisms.
Explanation
Due to its beneficial properties, syringic acid is being researched for its potential use in the development of pharmaceutical and cosmetic products.
Explanation
The chemical structure of syringic acid consists of a benzene ring fused to a 1,4-dioxane, which contributes to its unique properties and potential applications.
Class
Benzodioxans
Natural sources
Olives, grapes, and sesame seeds
Health benefits
Anti-inflammatory and antimicrobial effects
Research applications
Pharmaceutical and cosmetic industries
Chemical structure
Contains a benzene ring fused to a 1,4-dioxane
Check Digit Verification of cas no
The CAS Registry Mumber 873378-07-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,3,3,7 and 8 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 873378-07:
(8*8)+(7*7)+(6*3)+(5*3)+(4*7)+(3*8)+(2*0)+(1*7)=205
205 % 10 = 5
So 873378-07-5 is a valid CAS Registry Number.
873378-07-5Relevant academic research and scientific papers
A tautomeric ligand enables directed C-H hydroxylation with molecular oxygen
Li, Zhen,Wang, Zhen,Chekshin, Nikita,Qian, Shaoqun,Qiao, Jennifer X.,Cheng, Peter T.,Yeung, Kap-Sun,Ewing, William R.,Yu, Jin-Quan
, p. 1452 - 1457 (2021/06/30)
Hydroxylation of aryl carbon-hydrogen bonds with transition metal catalysts has proven challenging when oxygen is used as the oxidant. Here, we report a palladium complex bearing a bidentate pyridine/ pyridone ligand that efficiently catalyzes this reaction at ring positions adjacent to carboxylic acids. Infrared, x-ray, and computational analysis support a possible role of ligand tautomerization from monoanionic (L,X) to neutral (L,L) coordination in the catalytic cycle of aerobic carbon-hydrogen hydroxylation reaction. The conventional site selectivity dictated by heterocycles is overturned by this catalyst, thus allowing late-stage modification of compounds of pharmaceutical interest at previously inaccessible sites.
