113231-14-4 Usage
Explanation
This is an alternative name for 1,3-Benzenediol, 5-ethenyl-, which highlights the presence of a vinyl group attached to the catechol structure.
Explanation
The compound consists of a benzene ring (a six-carbon ring with alternating single and double bonds) with two hydroxyl (OH) groups at the 1 and 3 positions, and a vinyl group (a carbon-carbon double bond) attached to the 5 position.
Explanation
1,3-Benzenediol, 5-ethenylis used in the production of various industrial products, including dyes for coloring fabrics and plastics, adhesives for bonding materials, and polymers for creating plastics and other materials.
Explanation
This chemical compound serves as a building block or intermediate in the production of various pharmaceuticals, contributing to the development of new drugs and medications.
Explanation
1,3-Benzenediol, 5-ethenylis utilized as a chemical intermediate in organic chemistry, meaning it is a compound that is used to produce other compounds through chemical reactions.
Explanation
Due to its antioxidant properties, 1,3-Benzenediol, 5-ethenylis used in the formulation of skincare and cosmetic products to help protect the skin from damage caused by free radicals and oxidative stress.
Explanation
It is crucial to handle 1,3-Benzenediol, 5-ethenylwith care, as it can be harmful if accidentally ingested or inhaled. Additionally, it can cause irritation to the skin and eyes upon contact, necessitating proper safety measures during its use and storage.
Structure
Benzene ring with two hydroxyl groups and an attached vinyl group
Industrial applications
Dyes, adhesives, and polymers
Pharmaceutical synthesis
Used in the synthesis of pharmaceuticals
Chemical intermediate
Used in organic chemistry
Antioxidant properties
Used in skincare and cosmetic products
Safety precautions
Harmful if ingested or inhaled, causes skin and eye irritation
Check Digit Verification of cas no
The CAS Registry Mumber 113231-14-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,3,2,3 and 1 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 113231-14:
(8*1)+(7*1)+(6*3)+(5*2)+(4*3)+(3*1)+(2*1)+(1*4)=64
64 % 10 = 4
So 113231-14-4 is a valid CAS Registry Number.
113231-14-4Relevant articles and documents
A new efficient resveratrol synthesis
Guiso, Marcella,Marra, Carolina,Farina, Angela
, p. 597 - 598 (2002)
The (E)-3,4′,5-trihydroxystilbene (resveratrol) was synthesised via Heck reaction in few steps and with an overall 70% yield.
Phenolic Bis-styrylbenzo[ c]-1,2,5-thiadiazoles as Probes for Fluorescence Microscopy Mapping of Aβ Plaque Heterogeneity
Zhang, Jun,Konsmo, Audun,Sandberg, Alexander,Wu, Xiongyu,Nystr?m, Sofie,Obermüller, Ulrike,Wegenast-Braun, Bettina M.,Konradsson, Peter,Lindgren, Mikael,Hammarstr?m, Per
, p. 2038 - 2048 (2019/02/26)
A fluorescent bis-styryl-benzothiadiazole (BTD) with carboxylic acid functional groups (X-34/Congo red analogue) showed lower binding affinity toward Aβ1-42 and Aβ1-40 fibrils than its neutral analogue. Hence, variable patterns of neutral OH-substituted bis-styryl-BTDs were generated. All bis-styryl-BTDs showed higher binding affinity to Aβ1-42 fibrils than to Aβ1-40 fibrils. The para-OH on the phenyl rings was beneficial for binding affinity while a meta-OH decreased the affinity. Differential staining of transgenic mouse Aβ amyloid plaque cores compared to peripheral coronas using neutral compared to anionic bis-styryl ligands indicate differential recognition of amyloid polymorphs. Hyperspectral imaging of transgenic mouse Aβ plaque stained with uncharged para-hydroxyl substituted bis-styryl-BTD implicated differences in binding site polarity of polymorphic amyloid plaque. Most properties of the corresponding bis-styryl-BTD were retained with a rigid alkyne linker rendering a probe insensitive to cis-trans isomerization. These new BTD-based ligands are promising probes for spectral imaging of different Aβ fibril polymorphs.