5796-23-6 Usage
Molecular Weight
250.29 g/mol
Appearance
Colorless to pale yellow liquid or crystalline solid
Solubility
Soluble in organic solvents like ethanol, acetone, and diethyl ether; slightly soluble in water
Uses
a. Fragrance enhancer in perfumes
b. Flavoring agent in the food industry
c. Additive in cosmetics
Stability
More stable and less prone to oxidation than hydroquinone due to the addition of acetic acid groups
Shelf Life
Enhances the shelf life of products when added
Safety Precautions
a. Harmful if ingested
b. Avoid contact with skin and eyes
c. Handle with care and use appropriate protective equipment
Storage
Store in a cool, dry, and well-ventilated area, away from heat and direct sunlight
Regulatory Status
Subject to regulations and guidelines depending on the industry and region of use (e.g., FDA regulations for the food and cosmetics industry)
Check Digit Verification of cas no
The CAS Registry Mumber 5796-23-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,7,9 and 6 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 5796-23:
(6*5)+(5*7)+(4*9)+(3*6)+(2*2)+(1*3)=126
126 % 10 = 6
So 5796-23-6 is a valid CAS Registry Number.
5796-23-6Relevant academic research and scientific papers
Gold-catalyzed C-H oxidative polyacyloxylation reaction of hindered arenes
Pradal, Alexandre,Faudot Dit Bel, Pierre,Toullec, Patrick Y.,Michelet, Veronique
experimental part, p. 2463 - 2468 (2012/09/08)
The synthesis of polyacyloxylated aromatic derivatives was achieved in moderate yields using a gold-catalyzed C-H activation strategy and di(acetoxy)iodobenzene as an oxidant. Georg Thieme Verlag Stuttgart · New York.
Repetitive Diels-Alder Reactions for the Growth of Linear Polyacenequinoid Derivatives
Thomas, Alan D.,Miller, Larry L.
, p. 4160 - 4169 (2007/10/02)
Starting from 2,3,5,6-tetramethylidene-7-oxanorbornane, repetitive quinone Diels-Alder/oxidation reactions produced a series of epoxypolyacenequinones with up to eleven linearly annulated rings.Epoxide ring opening-oxidation gave polyacenequinones with se
