119229-91-3 Usage
Chemical structure
A compound consisting of a benzene ring with two hydroxyl groups and two acetyl groups, a vinyl group, and two phenyl rings with acetyl groups.
Synonyms
Resorcinol diacetate, 4-[(1E)-2-[3,5-bis(acetyloxy)phenyl]ethenyl]-, diacetate
Appearance
A crystalline solid or amorphous powder
Solubility
Soluble in organic solvents such as ethanol, methanol, and acetone
Stability
Stable under normal temperature and pressure conditions, but may decompose upon exposure to heat or strong acids
Reactivity
Can undergo various chemical reactions, such as esterification, hydrolysis, and condensation
Pharmaceuticals
Used in the production of various pharmaceuticals
Dyes
Utilized in the synthesis of dyes
Industrial products
Employed in the production of other industrial products
Polymer synthesis
Used as a monomer in the synthesis of polymers
Rubber industry
Acts as a cross-linking agent
Biomedicine
Potential applications in drug delivery systems and biomaterials
Safety
Handle with care, as it may cause irritation to the eyes, skin, and respiratory system. Wear appropriate personal protective equipment (PPE) when working with this compound.
Storage
Store in a cool, dry, and well-ventilated area, away from heat, sparks, and open flames. Keep the container tightly closed when not in use.
Regulatory status
May be subject to specific regulations and restrictions depending on the country or region, particularly in the context of pharmaceuticals, dyes, and industrial applications.
Check Digit Verification of cas no
The CAS Registry Mumber 119229-91-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,9,2,2 and 9 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 119229-91:
(8*1)+(7*1)+(6*9)+(5*2)+(4*2)+(3*9)+(2*9)+(1*1)=133
133 % 10 = 3
So 119229-91-3 is a valid CAS Registry Number.
119229-91-3Relevant articles and documents
Oxyresveratrol: Structural modification and evaluation of biological activities
Chatsumpun, Nutputsorn,Chuanasa, Taksina,Sritularak, Boonchoo,Lipipun, Vimolmas,Jongbunprasert, Vichien,Ruchirawat, Somsak,Ploypradith, Poonsakdi,Likhitwitayawuid, Kittisak
, (2016)
Oxyresveratrol (2,4,3' ,5' -tetrahydroxystilbene, 1), a phytoalexin present in large amounts in the heartwood of Artocarpus lacucha Buch.-Ham., has been reported to possess a wide variety of biological activities. As part of our continuing studies on the structural modification of oxyresveratrol, a library of twenty-six compounds was prepared via O-alkylation, aromatic halogenation, and electrophilic aromatic substitution. The two aromatic rings of the stilbene system of 1 can be chemically modulated by exploiting different protecting groups. Such a strategy allows for selective and exclusive modifications on either ring A or ring B. All compounds were evaluated in vitro for a panel of biological activities, including free radical scavenging activity, DNA protective properties, antiherpetic activity, inhibition of α-glucosidase and neuraminidase, and cytotoxicity against some cancer cell lines. Several derivatives were comparably active or even more potent than the parent oxyresveratrol and/or the appropriate positive controls. The partially etherified analogs 5' -hydroxy-2,3' ,4-trimethoxystilbene and 3' ,5' -dihydroxy-2,4-dimethoxystilbene demonstrated promising anti-herpetic and DNA protective activities, offering new leads for neuropreventive agent research, whereas 5' -hydroxy-2,3' ,4,-triisopropoxystilbene displayed anti-α-glucosidase effects, providing a new lead molecule for anti-diabetic drug development. 3' ,5' -Diacetoxy-2,4-diisopropoxystilbene showed potent and selective cytotoxicity against HeLa cancer cells, but the compound still needs further in vivo investigation to verify its anticancer potential.
