87861-81-2 Usage
Guanidine group
A positively charged functional group that contributes to the compound's antimicrobial and antifungal properties.
Hexoxyphenyl moiety
A lipophilic group that aids in the compound's solubility and interaction with other molecules.
Antimicrobial properties
The ability to inhibit the growth of microorganisms, making it useful in pharmaceuticals and cosmetics.
Antifungal properties
The capacity to prevent the growth of fungi, which is beneficial in various personal care products.
Cosmetic applications
Incorporated into cosmetic products to provide antimicrobial and antifungal benefits, ensuring product safety and efficacy.
Aromatic structure
A benzene ring with a methyl group attached, which contributes to the compound's stability and reactivity.
Sulfonic acid group
A strong acidic functional group that enables the compound to act as a catalyst in various chemical reactions.
Reagent in organic synthesis
Utilized as a starting material or intermediate in the synthesis of other organic compounds.
Production of dyes and pigments
Involved in the manufacturing process of colorants for various industries, including textiles, plastics, and printing.
Pharmaceutical applications
Used in the synthesis of active pharmaceutical ingredients and as a catalyst in drug production processes.
Check Digit Verification of cas no
The CAS Registry Mumber 87861-81-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,8,6 and 1 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 87861-81:
(7*8)+(6*7)+(5*8)+(4*6)+(3*1)+(2*8)+(1*1)=182
182 % 10 = 2
So 87861-81-2 is a valid CAS Registry Number.
87861-81-2Relevant academic research and scientific papers
Novel N-hydroxyguanidine derivatives as anticancer and antiviral agents
Tai,Lien,Lai,Khwaja
, p. 236 - 238 (2007/10/02)
Hydroxyguanidine contains both features of guanidine and hydroxyurea and has antiviral and anticancer activities both in vitro and in vivo. In order to enhance the antiviral and anticancer activity of this compound, a new series of hydroxyguanidine deriva