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2,4-Dihydroxy-3-formyl-6-methylbenzoic acid ethyl ester is a chemical compound with the molecular formula C11H12O5. It is an ethyl ester derivative of 2,4-dihydroxy-3-formyl-6-methylbenzoic acid, characterized by its pale yellow, viscous liquid appearance and a fruity, sweet aroma. 2,4-Dihydroxy-3-formyl-6-methylbenzoic acid ethyl ester is known for its potential antioxidant and anti-inflammatory properties, which make it a promising candidate for various applications in the pharmaceutical and cosmetic industries, as well as in the synthesis of other organic compounds.

39503-14-5

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39503-14-5 Usage

Uses

Used in Flavoring and Fragrance Industry:
2,4-Dihydroxy-3-formyl-6-methylbenzoic acid ethyl ester is used as a flavoring agent and fragrance ingredient in the food and cosmetic industry due to its distinctive fruity, sweet aroma. Its unique scent profile makes it a valuable addition to a wide range of products, enhancing their sensory appeal and consumer experience.
Used in Pharmaceutical Applications:
2,4-Dihydroxy-3-formyl-6-methylbenzoic acid ethyl ester is used as a potential pharmaceutical candidate for its antioxidant and anti-inflammatory properties. Its ability to combat oxidative stress and reduce inflammation makes it a promising agent for the development of treatments for various diseases and conditions, including those associated with chronic inflammation and oxidative damage.
Used in Cosmetic Applications:
In the cosmetic industry, 2,4-Dihydroxy-3-formyl-6-methylbenzoic acid ethyl ester is used for its potential antioxidant and anti-inflammatory properties, which can contribute to skin health and protection. Its incorporation into cosmetic formulations may help to reduce signs of aging, inflammation, and oxidative stress, promoting a healthier and more youthful appearance.
Used in Organic Synthesis:
2,4-Dihydroxy-3-formyl-6-methylbenzoic acid ethyl ester is also used in the synthesis of various other organic compounds. Its unique chemical structure allows it to serve as a versatile building block in the creation of new molecules with potential applications in various fields, including pharmaceuticals, materials science, and agrochemicals.
Found in Natural Plant Extracts:
2,4-Dihydroxy-3-formyl-6-methylbenzoic acid ethyl ester can be found in some natural plant extracts, highlighting its potential as a naturally occurring compound with beneficial properties. Its presence in plants may contribute to the overall health-promoting effects of these natural sources and provide a basis for further research into its applications and benefits.

Check Digit Verification of cas no

The CAS Registry Mumber 39503-14-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,9,5,0 and 3 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 39503-14:
(7*3)+(6*9)+(5*5)+(4*0)+(3*3)+(2*1)+(1*4)=115
115 % 10 = 5
So 39503-14-5 is a valid CAS Registry Number.
InChI:InChI=1/C11H12O5/c1-3-16-11(15)9-6(2)4-8(13)7(5-12)10(9)14/h4-5,13-14H,3H2,1-2H3

39503-14-5SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 3-formyl-2,4-dihydroxy-6-methylbenzoate

1.2 Other means of identification

Product number -
Other names 3-formyl-2,4-dihydroxy-6-methyl-benzoic acid ethyl ester

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:39503-14-5 SDS

39503-14-5Relevant academic research and scientific papers

Synthesis of new Lichen tridepsides

Elix, John A.,Jayanthi, Vilas K.,McCaffery, Leslie F.,Yu, Jin

, p. 1045 - 1052 (2007/10/03)

The unambiguous total synthesis of ten O-methyl and/or C-hydroxy derivatives of gyrophoric acid (1) has been achieved by using the condensation of an appropriately substituted benzole acid and benzyl lecanorate (33) or benzyl 2-O-methyllecanorate (32) in the key step.

3-Hydroxyumbilicaric Acid and 3-Methoxyumbilicaric Acid, New Tridepsides from the Lichen Parmelinopsis bonariensis

Elix, John A.,Jin, Yu,Adler, Monica T.

, p. 765 - 770 (2007/10/02)

The new tridepsides 3-hydroxyumbilicaric acid (4) and 3-methoxyumbilicaric acid (5) have been detected in the lichen Parmelinopsis bonariensis and the structures established by unambiguous synthesis.

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