6318-65-6 Usage
Description
(Acetyloxy)methyl 2-hydroxybenzoate, also known as methyl acetoxymethyl salicylate, is a chemical compound with the molecular formula C11H12O5. It is a versatile ingredient that finds applications in various industries due to its unique properties.
Uses
Used in Cosmetic and Pharmaceutical Industries:
(Acetyloxy)methyl 2-hydroxybenzoate is used as an active ingredient in skincare and topical pain relief products for its anti-inflammatory and analgesic properties. It helps in alleviating muscle and joint pain, making it a valuable component in these applications.
Used in Food Industry:
(Acetyloxy)methyl 2-hydroxybenzoate is used as a flavoring agent in the food products industry. Its unique taste profile contributes to the enhancement of flavors in various food items.
Used in Perfumes and Personal Care Products:
In the perfumery and personal care products industry, (acetyloxy)methyl 2-hydroxybenzoate is used as a fragrance ingredient. Its distinct scent adds a pleasant aroma to perfumes and personal care products, making it a sought-after component in these applications.
Check Digit Verification of cas no
The CAS Registry Mumber 6318-65-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,3,1 and 8 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 6318-65:
(6*6)+(5*3)+(4*1)+(3*8)+(2*6)+(1*5)=96
96 % 10 = 6
So 6318-65-6 is a valid CAS Registry Number.
6318-65-6Relevant articles and documents
Evaluation of glycolamide esters and various other esters of aspirin as true aspirin prodrugs
Nielsen,Bundgaard
, p. 727 - 734 (2007/10/02)
A series of glycolamide, glycolate, (acyloxy)methyl, alkyl, and aryl esters of acetylsalicylic acid (aspirin) were synthesized and evaluated as potential prodrug forms of aspirin. N,N-Disubstituted glycolamide esters were found to be rapidly hydrolized in human plasma, resulting in the formation of aspirin as well as the corresponding salicylate esters. These in turn hydrolyzed rapidly to salicylic acid. The largest amount of aspirin formed from the esters were 50 and 55% in case of the N,N-dimethyl- and N,N-diethylglycolamide esters, respectively. Similar results were obtained in blood with the N,N-dimethyl- and N,N-diethylglycolamide esters. Unsubstituted and monosubstituted glycolamide esters as well as most other esters previously suggested to be aspirin prodrugs were shown to hydrolyze exclusively to the corresponding salicylic acid esters. Lipophilicity parameters and water solubilities of the esters were determined, and structural factors favoring ester prodrug hydrolysis at the expense of deacetylation to yield salicylate ester are discussed. The properties of some N,N-disubstituted glycolamide esters of aspirin are highlighted with respect to their use as potential aspirin prodrugs.
