944060-98-4 Usage
Description
Methyl 2-mercapto-6-methoxybenzoate, also known as thiomethyl salicylate, is a chemical compound with a molecular formula C9H10O3S. It is characterized by its strong, sweet, and floral odor.
Uses
Used in Fragrance Industry:
Methyl 2-mercapto-6-methoxybenzoate is used as a fragrance ingredient for its strong, sweet, and floral scent in various personal care products and perfumes.
Used in Food and Beverage Industry:
Methyl 2-mercapto-6-methoxybenzoate is used as a flavoring agent to enhance the taste and aroma of food products and beverages.
Used in Pharmaceutical Industry:
Methyl 2-mercapto-6-methoxybenzoate is studied for its potential therapeutic properties, such as antioxidant and anti-inflammatory effects, which may contribute to the development of new treatments and medications.
Check Digit Verification of cas no
The CAS Registry Mumber 944060-98-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,4,4,0,6 and 0 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 944060-98:
(8*9)+(7*4)+(6*4)+(5*0)+(4*6)+(3*0)+(2*9)+(1*8)=174
174 % 10 = 4
So 944060-98-4 is a valid CAS Registry Number.
944060-98-4Relevant articles and documents
Synthesis and structure activity relationship studies of benzothieno[3,2-b]furan derivatives as a novel class of IKKβ inhibitors
Sugiyama, Hideyuki,Yoshida, Masato,Mori, Kouji,Kawamoto, Tomohiro,Sogabe, Satoshi,Takagi, Terufumi,Oki, Hideyuki,Tanaka, Toshimasa,Kimura, Hiroyuki,Ikeura, Yoshinori
, p. 613 - 624 (2007)
As a novel class of IKKβ inhibitors, a series of tricyclic furan derivatives was designed and synthesized based on the structure of known thiophene IKKβ inhibitors. Among the various fused furan derivatives synthesized, a benzothieno[3,2-b]furan derivative 13a displayed potent inhibitory activity towards IKKβ in enzymatic and cellular assays. The potent inhibitory activity originates from an intramolecular non-bonded S...O interaction which was confirmed by the X-ray structure of JNK3 with 16k. The introduction of further substituents on the core structure led to the discovery of the 6-alkoxy derivatives, which possessed a comparable IKKβ inhibitory activity to 13a and an improved metabolic stability. Among these, appropriately lipophilic compounds 16a, h, i, and 13g (logD>2) were found to possess good oral bioavailability.
