83194-70-1

Usage

Uses

Used in Food Industry:
2,6-diMethyl-4-hydroxybenzoic acid Methyl ester is used as a food preservative and flavoring agent for its ability to extend the shelf life and enhance the taste of various food products.
Used in Personal Care and Cosmetics Industry:
2,6-diMethyl-4-hydroxybenzoic acid Methyl ester is used as an antimicrobial and antioxidant agent in the formulation of personal care products and cosmetics, helping to protect the products from microbial contamination and oxidation, thus ensuring their safety and efficacy.
Used in Pharmaceutical Industry:
2,6-diMethyl-4-hydroxybenzoic acid Methyl ester is used in the production of pharmaceuticals due to its antimicrobial and antioxidant properties, which can contribute to the stability and effectiveness of medications.
Used in Fragrance Industry:
2,6-diMethyl-4-hydroxybenzoic acid Methyl ester is used as a component in the production of fragrances, providing a unique scent and enhancing the overall aroma of perfumes and other scented products.
Used in Sunscreen Products:
2,6-diMethyl-4-hydroxybenzoic acid Methyl ester is used as a UV filter in sunscreen products, offering protection against harmful ultraviolet radiation and helping to prevent skin damage.
It is important to handle 2,6-diMethyl-4-hydroxybenzoic acid Methyl ester with care, as it can be harmful if swallowed, inhaled, or comes into contact with the skin. Proper safety measures should be taken during its use and production to minimize potential risks.

InChI:InChI=1/C10H12O3/c1-6-4-8(11)5-7(2)9(6)10(12)13-3/h4-5,11H,1-3H3

Upstream product

• 107941-44-6 methyl 8,8-dimethoxy-1,5-dimethyl-3-oxo-2-oxabicyclo<2.2.2>oct-5-ene-6-carboxylate 
• 67333-67-9 methyl 2,6-dimethyl-4-oxo-2-cyclohexene-1-carboxylate 
• 14920-81-1 methyl 2,6-dimethylbenzoate 
• 75056-97-2 2,6-dimethyl-4-hydroxybenzoic acid 
• 74-88-4 methyl iodide 
• 306297-02-9 4-benzyloxy-2,6-dimethylbenzoic acid methyl ester 

Downstream Products

• 1351163-90-0 methyl 2,6-dimethyl-4-{[(2S)-4-methyl-3,4-dihydro-2H-1,4-benzoxazin-2-yl]methoxy}benzoate 
• 1116624-25-9 2,6-dimethyl-4-{[(2S)-4-methyl-3,4-dihydro-2H-1,4-benzoxazin-2-yl]methoxy}benzoic acid 
• 848846-87-7 2,6-dimethyl-4-{[(2S)-4-methyl-3,4-dihydro-2H-1,4-benzoxazin-2-yl]methoxy}benzoyl chloride 
• 848846-61-7 2-{4-chloro-3-[(2,6-dimethyl-4-{[(2S)-4-methyl-3,4-dihydro-2H-1,4-benzoxazin-2-yl]methoxy}benzoyl)amino]phenyl}-2-methylpropanoic acid 
• 1356963-67-1 C₂₈H₂₉ClN₂O₅ 
• 1258975-01-7 methyl 2,6-dimethyl-4-octylbenzoate 
• 306297-03-0 methyl 2,6-dimethyl-4-(trifluoromethylsulfonyloxy)benzoate 

Relevant academic research and scientific papers

Facile Synthesis of Halogen Decorated para -/ meta -Hydroxybenzoates by Iridium-Catalyzed Borylation and Oxidation

Hydroxybenzoates are an important class of phenols that are widely used as preservatives and antiseptics in the food and pharmaceutical industries. In this report, a facile preparation of 2,6- and 2,3-disubstituted 4/5-hydroxybenzoates by iridium-catalyze

COMPOUNDS AND METHODS FOR REGULATING INSULIN SECRETION

Disclosed herein are methods for inducing insulin secretion in a glucose-dependent manner and compounds for use in these methods.

METHOD OF MANUFACTURING 4-HYDROXY-2-METHYLBENZOIC ACID DERIVATIVE

PROBLEM TO BE SOLVED: To provide a method for manufacturing 4-hydroxy-2-methylbenzoic esters simply in a short time. SOLUTION: There is provided a method for manufacturing a 4-hydroxy-2-methylbenzoic acid derivative (1) by air oxidizing a 2-methyl-4-oxo-2

Copper(II)-catalyzed aromatization followed by bromination of cyclohexenones leading to phenols and bromophenols

Conversion of substituted cyclohexenones into the corresponding phenols can be achieved using copper acetate as the catalyst in the presence of LiBr and CF3COOH under oxygen. With the use of excess LiBr, electrophilic aromatic bromination afforded the corresponding bromophenol under similar catalytic conditions. Copyright

The use of Hagemann's Esters to prepare highly functionalized phenols and benzenes

Hagemann's esters can be converted into highly functionalized phenols or arenes. The systematic functionalization of Hagemann's ester derivatives permits the preparation of tri-and tetraalkyl-substituted phenols or tetra-, penta-, and hexaalkyl-substituted benzenes. Kotnis's aromatization procedure was found to be solvent dependent, and Suzuki couplings were found to be sensitive to steric hindrance. Wittig olefination and ortho-Claisen reactions were reliable means to introduce alkyl substituents at C-4 and/or C-5 positions, respectively. The acid-promoted dehydration of tertiary alcohol 46 to produce enone 47, followed by its selective alkylation (cf. 48) is new. ARKAT USA, Inc.

PIPERAZINE DERIVATIVES USEFUL AS CCR5 ANTAGONISTS

The use is described of CCR5 antagonists of formula (I) or a pharmaceutically acceptable salt thereof, wherein: R is optionally substituted phenyl, pyridyl, thiophenyl or naphthyl; R 1 is hydrogen or alkyl; R 2 is substituted phenyl, substituted heteroary

Piperazine derivatives useful as CCR5 antagonists

The use of CCR5 antagonists of the formula or a pharmaceutically acceptable salt thereof, wherein R is optionally substituted phenyl, pyridyl, thiophenyl or naphthyl; R1is hydrogen or alkyl; R2is substituted phenyl, substituted heter

PREPARATION AND CYCLOADDITION OF FUNCTIONALIZED 4,6-DIALKYLPYRONE-5-CARBOXYLATES. SYNTHESIS OF BICYCLIC LACTONES AND SUBSTITUTED BENZOATES

Several alkyl pyrone-5-carboxylates (coumalates) with alkyl and functionalized alkyl substituents at C4 and C6 have been prepared by a general route; their cycloadditions with electron-rich olefins have been carried out to provide aromatic and non-aromati