4906-69-8

Usage

Uses

Used in Cosmetic and Pharmaceutical Products:
Methyl salicylate is used as a fragrance and soothing agent in cosmetic and pharmaceutical products due to its pleasant aroma and calming effects on the skin.
Used in Flavoring Agents for Food and Beverages:
Methyl salicylate is utilized as a flavoring agent in food and beverages, imparting a unique taste and enhancing the overall sensory experience.
Used in Topical Pain Relief Treatments:
Leveraging its analgesic and anti-inflammatory properties, methyl salicylate is commonly found in topical pain relief treatments, providing relief from muscle aches and joint pain.
Used in Perfume and Personal Care Product Production:
Methyl salicylate is employed in the production of perfumes, soaps, and other personal care products, contributing to their pleasant odor and enhancing their appeal to consumers.

InChI:InChI=1/C14H12O3/c1-17-14(16)12-9-5-8-11(13(12)15)10-6-3-2-4-7-10/h2-9,15H,1H3

Upstream product

• 186581-53-3 diazomethane 
• 304-06-3 3-phenylsalicylic acid 
• 108-90-7 chlorobenzene 
• 1037435-86-1 C₁₇H₂₈O₃Si₂ 
• 102-52-3 malonaldehydebis(dimethylacetal) 
• 75073-98-2 dimethyl (E)-2-styrylcyclopropane-1,1-dicarboxylate 
• 90-43-7 2-Phenylphenol 
• 417698-00-1 O-2-biphenylyl N-isopropylcarbamate 
• 67-56-1 methanol 
• 117369-89-8 methyl 3-oxo-4-phenylhept-6-enoate 
• 77-78-1 dimethyl sulfate 

Downstream Products

• 4432-97-7 2-hydroxy-biphenyl-3-carboxylic acid amide 
• 131-90-8 2-hydroxy-biphenyl-3-carboxylic acid butylamide 
• 178547-23-4 methyl 2-benzyloxy-3-phenylbenzoate 
• 63906-82-1 2-(2-hydroxy-ethoxy)-biphenyl-3-carboxylic acid amide 
• 63887-18-3 2-allyloxy-biphenyl-3-carboxylic acid amide 
• 63906-86-5 2-methoxy-biphenyl-3-carboxylic acid amide 
• 100482-21-1 3-Phenyl-2-(2-diaethylamino-aethoxy)-benzamid 
• 154447-37-7 8-phenyl-2-thiomorpholin-4-yl-chromen-4-one 
• 154447-39-9 8-phenyl-2-piperidin-1-yl-chromen-4-one 
• 154447-36-6 LY 294002 
• 63992-48-3 2-hydroxy-biphenyl-3-carboxylic acid-(2-hydroxy-ethylamide) 

Relevant academic research and scientific papers

Cascade dimerization of 2-styryl-1,1-cyclopropanedicarboxylate upon treatment with gallium trichloride

2-Styrylcyclopropane-1,1-dicarboxylate treated with anhydrous gallium trichloride undergoes dimerization with the cyclopropane ring opening and the styryl substituent double bond involvement, leading to the formation of polysubstituted cyclic and bicyclic structures with the predominance of the former or the latter depending on the reaction conditions. Most compounds are formed with very high diastereoselectivity. Thirteen major and minor dimeric structures were isolated and reliably characterized, two of which were found to additionally include a chlorine atom. A rare for the reactions of donor-acceptor cyclopropanes example of the formation of a product with the fused cyclobutane ring was effected at–80 °C. Plausible mechanisms of observed processes were discussed.

Anticancer agent synthesis designed by artificial intelligence: Pd(OAc)2-catalyzed one-pot preparation of biphenyls and its application to a concise synthesis of various diazofluorenes

We successfully synthesized the antitumor agent 1-methoxydiazofluorene via an artificial intelligence (AI)-proposed design. The pivotal biphenyl scaffold of 1-methoxydiazofluorene was constructed by applying Pd(OAc)2-catalyzed cycloaromatizatio

Regioselective synthesis of functionalized biaryls based on the first [3+3] cyclocondensations of 4-Aryl-1,3-bis(trimethylsilyloxy)buta-1,3-dienes

Sterically encumbered biaryls were regioselectively prepared by formal [3+3] cyclocondensations of novel 4-aryl-1,3- bis(trimethylsilyloxy)-1,3-dienes. Georg Thieme Verlag Stuttgart · New York.

Substitution of hydroxybiaryls via directed ortho-lithiation of N-silylated O-aryl N-isopropylcarbamates

Herein we report regioselective substitution reactions of a series of 2- and 3-hydroxybiaryls including BINOL via a new directed ortho-metalation procedure. O-Aryl N-isopropylcarbamates, conveniently prepared from phenols and isopropyl isocyanate, are tem

Synthetic studies of the phosphatidylinositol 3-kinase inhibitor LY294002 and related analogues

Synthetic methodologies have been developed for the direct and high-yielding preparation of the phosphatidyl-inositol 3-kinase inhibitor LY294002. These methods are readily amenable to the efficient generation of analogues, which will facilitate a detailed investigation of this important family of enzymes.