16846-10-9

Usage

Uses

Used in Fragrance and Flavoring Industry:
METHYL 2,6-DIHYDROXY-4-METHYLBENZOATE is used as a fragrance and flavoring agent for its sweet, floral scent, adding pleasant aromas to perfumes, cosmetics, and food items.
Used in Cosmetics Industry:
In the cosmetics industry, METHYL 2,6-DIHYDROXY-4-METHYLBENZOATE is used as an ingredient to enhance the sensory experience of products, leveraging its pleasant odor.
Used in Food Industry:
METHYL 2,6-DIHYDROXY-4-METHYLBENZOATE is used as a flavoring agent in the food industry to impart a desirable taste and aroma to various food products.
Used as a UV Filter in Sunscreen Products:
METHYL 2,6-DIHYDROXY-4-METHYLBENZOATE is used as a UV filter in sunscreen products, capitalizing on its antioxidant properties to protect the skin from harmful ultraviolet radiation.
It is crucial to handle METHYL 2,6-DIHYDROXY-4-METHYLBENZOATE with care due to its potential to cause irritation to the skin, eyes, and respiratory system if not used properly.

InChI:InChI=1/C9H10O4/c1-5-3-6(10)8(7(11)4-5)9(12)13-2/h3-4,10-11H,1-2H3

Upstream product

• 186581-53-3 diazomethane 
• 480-67-1 2,6-dihydroxy-4-methyl-benzoic acid 
• 504-15-4 orcinol 
• 74-88-4 methyl iodide 
• 77-78-1 dimethyl sulfate 

Downstream Products

• 16846-20-1 3-formyl-2,6-dihydroxy-4-methyl-benzoic acid methyl ester 
• 54130-89-1 2,6-dimethoxy-4-methyl-benzoic acid methyl ester 
• 57439-16-4 methyl 2-hydroxy-6-methoxy-4-methylbenzoate 
• 114561-50-1 acide hydroxy-2-methoxy-6-methyl-4-benzoique 
• 329317-39-7 4-methyl-2,6-bis-(2-nitro-4-trifluoromethanesulfonyl-phenoxy)-benzoic acid methyl ester 
• 17492-27-2 methyl-2,6-diacetyloxy-4-methyl benzoate 
• 73855-52-4 3-chloro-2,6-dihydroxy-4-methyl-benzoic acid 
• 73855-53-5 3,5-dichloro-2,6-dihydroxy-4-methyl-benzoic acid 
• 247086-79-9 5-benzyloxy-2-(2,6-bis-benzyloxy-4-methyl-benzoyl)-3-methoxy-benzoic acid 
• 178749-80-9 2,6-bis-benzyloxy-4-methyl-benzoic acid 5-benzyloxy-2-bromo-3-methoxy-benzyl ester 
• 247086-81-3 (4-benzyloxy-2-hydroxymethyl-6-methoxy-phenyl)-(2,6-bis-benzyloxy-4-methyl-phenyl)-methanone 
• 178749-82-1 5-benzyloxy-2-(2,6-bis-benzyloxy-4-methyl-benzoyl)-3-methoxy-benzoic acid methyl ester 
• 178749-81-0 5-benzyloxy-2-(2,6-bis-benzyloxy-4-methyl-benzoyl)-3-methoxy-benzaldehyde 
• 23565-79-9 2,6-bis-benzyloxy-4-methyl-benzoic acid 

Relevant academic research and scientific papers

Reactions of fused and unfused α-pyrones with magnesium alkoxide, sodium alkoxide and water as the nucleophile: effects of chelation

The reactions between a series of α-pyrones (two mono- and three fused) and the non-chelating base sodium alkoxide, the chelating base magnesium alkoxide and water as the nucleophile, have been studied.Aromatic and other products formed reflect the points of attack on the pyrone systems and when sodium methoxide is used the ensuing cyclisation is preferentially by aldol mechanisms.The employment of excess magnesium methoxide or ethoxide gives magnesium-chelated precursors and the nature of products now depends on these intermediates, and the protection afforded by such magnesium chelation to the reaction products.In the case of structures containing chelated β-keto ester features the chelates are screened from attack as aldol acceptors, but are effective Claisen acceptors.In such chelates an adjacent methylene is activated by further magnesium alkoxide to act as an aldol or Claisen donor.These contrasting aldol/Claisen reactivities, as between a non-chelating and a chelating base, are illustrated in the ensuing chemistry of the pyrones.Treatment with water releases the main carbon chain with decarboxylation, from which new products may form.

Method of preparing p-orsellinic acid esters

Resorcinols of the structure of p-orsellinic acid ester are obtained from pyrones of the formula STR1 by the action of no more than catalytic amounts of bases.