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2-(3,4-dihydroxy-5-methoxyphenyl)acetic acid, also known as vanillic acid, is a naturally occurring organic compound belonging to the phenolic acid family. It is characterized by a molecular formula of C8H8O5 and a molecular weight of 184.15 g/mol. 2-(3,4-dihydroxy-5-methoxyphenyl)acetic acid features a phenyl ring with three hydroxyl groups at the 3rd and 4th positions and a methoxy group at the 5th position, attached to a two-carbon acetic acid chain. Vanillic acid is widely found in plants, particularly in the seeds and pods of vanilla beans, and is also present in various fruits, vegetables, and beverages. It exhibits antioxidant, anti-inflammatory, and antimicrobial properties, making it a valuable compound in the food, pharmaceutical, and cosmetic industries. Additionally, vanillic acid serves as a precursor in the synthesis of vanillin, the primary component responsible for the characteristic aroma and flavor of vanilla.

2989-10-8

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2989-10-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2989-10-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,9,8 and 9 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 2989-10:
(6*2)+(5*9)+(4*8)+(3*9)+(2*1)+(1*0)=118
118 % 10 = 8
So 2989-10-8 is a valid CAS Registry Number.

2989-10-8Downstream Products

2989-10-8Relevant academic research and scientific papers

Tyrosinase and Layer-by-Layer supported tyrosinases in the synthesis of lipophilic catechols with antiinfluenza activity

Bozzini, Tiziana,Botta, Giorgia,Delfino, Michela,Onofri, Silvano,Saladino, Raffaele,Amatore, Donatella,Sgarbanti, Rossella,Nencioni, Lucia,Palamara, Anna Teresa

, p. 7699 - 7708 (2013)

Catechol derivatives with lipophilic properties have been selectively synthesized by tyrosinase in high yield avoiding long and tedious protection/deprotection steps usually required in traditional procedures. The synthesis was effective also with immobilized tyrosinase able to perform for more runs. The novel catechols were evaluated against influenza A virus, that continue to represent a severe threat worldwide. A significant antiviral activity was observed in derivatives characterized by antioxidant activity and long carbon alkyl side-chains, suggesting the possibility of a new inhibition mechanism based on both redox and lipophilic properties.

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