CAS 2150-44-9

3,5-Dihydroxybenzoic acid methyl ester

Description:

3,5-Dihydroxybenzoic acid methyl ester, with the CAS number 2150-44-9, is an organic compound characterized by its aromatic structure featuring two hydroxyl (-OH) groups and a methoxy (-OCH3) group attached to a benzoic acid framework. This compound is a methyl ester derivative of 3,5-dihydroxybenzoic acid, which contributes to its solubility in organic solvents. It typically appears as a white to off-white crystalline solid. The presence of hydroxyl groups imparts polar characteristics, making it capable of forming hydrogen bonds, which can influence its reactivity and interactions with other molecules. This compound is of interest in various fields, including pharmaceuticals and biochemistry, due to its potential biological activities, such as antioxidant properties. Additionally, it may serve as an intermediate in organic synthesis or as a reagent in chemical reactions. Proper handling and storage are essential, as with many organic compounds, to ensure safety and stability.

Formula: C₈H₈O₄

InChI: InChI=1S/C8H8O4/c1-12-8(11)5-2-6(9)4-7(10)3-5/h2-4,9-10H,1H3

InChI key: InChIKey=RNVFYQUEEMZKLR-UHFFFAOYSA-N

SMILES: C(OC)(=O)C1=CC(O)=CC(O)=C1

Synonyms:

• 3,5-Dihydroxy-benzoic aci methyl ester
• 3,5-Dihydroxybenzoic acid methyl ester
• 3,5-Dihydroxymethylbenzoate
• Benzoic acid, 3,5-dihydroxy-, methyl ester
• Methyl 3,5-hydroxybenzoate
• Methyl α-resorcylate
• NSC 61082
• α-Resorcinol carboxylic acid methyl ester
• α-Resorcylic acid, methyl ester
• Methyl 3,5-dihydroxybenzoate

Methyl 3,5-Dihydroxybenzoate

CAS: 2150-44-9

Formula: C₈H₈O₄

Purity: >98.0%(GC)

Color and Shape: White to Light yellow to Light orange powder to crystal

Molecular weight: 168.15

Ref: 3B-D2215

Methyl 3,5-dihydroxybenzoate, 98%

CAS: 2150-44-9

Methyl 3,5-dihydroxybenzoate was used in the synthesis of cored dendrimers. It was also used in the preparation of bis(5-carbomethoxy-1,3-phenylene)-32-crown-10, a semi-rigid 32-membered ring diester crown ether. It has been used to study ribonucleotide reductase inhibiton and anti-tumor activity .

Formula: C₈H₈O₄

Purity: 98%

Color and Shape: White to cream or pale brown, Crystals or powder or crystalline powder

Molecular weight: 168.15

Ref: 02-A15224

Methyl 3,5-dihydroxybenzoate

CAS: 2150-44-9

Methyl 3,5-dihydroxybenzoate

Formula: C₈H₈O₄

Purity: 99.5%

Molecular weight: 168.15

Ref: 54-BUP19152

Methyl 3,5-dihydroxybenzoate

CAS: 2150-44-9

Methyl 3, 5-dihydroxybenzoate was used in the synthesis of cored dendrimers.

Formula: C₈H₈O₄

Purity: 99.68%

Color and Shape: White To Off-White Crystalline Powder

Molecular weight: 168.1467

Ref: TM-T1355

Methyl 3,5-dihydroxybenzoate

CAS: 2150-44-9

Methyl 3,5-dihydroxybenzoate

Formula: C₈H₈O₄

Purity: ≥95%

Color and Shape: Pale yellow Solid

Molecular weight: 168.14671

Ref: 54-OR24884

Methyl 3,5-dihydroxybenzoate

CAS: 2150-44-9

Formula: C₈H₈O₄

Purity: 98%

Color and Shape: Solid

Molecular weight: 168.1467

Ref: IN-DA003RQH

Methyl 3,5-dihydroxybenzoate

CAS: 2150-44-9

Methyl 3,5-dihydroxybenzoate

Formula: C₈H₈O₄

Purity: 98%

Molecular weight: 168.15

Ref: IN-DG6422

Methyl 3,5-dihydroxybenzoate

CAS: 2150-44-9

Formula: C₈H₈O₄

Purity: 98%

Color and Shape: Solid

Molecular weight: 168.148

Ref: 10-F238758

3,5-Dihydroxybenzoic Acid Methyl Ester

Controlled Product

CAS: 2150-44-9

Applications The methyl ester of 3,5-Dihydroxybenzoic Acid (D451700) with potential antifeedant activity for pine weevil, Hylobius abietis.
References Sunnerheim, K. et al.: J. Agric. Food Chem., 55, 9365 (2007); Tung, Y.-T. et al.: Biores. Technol., 98, 1120 (2007);

Formula: C₈H₈O₄

Color and Shape: Neat

Molecular weight: 168.15

Ref: TR-D451715

3,5-Dihydroxybenzoic acid methyl ester

CAS: 2150-44-9

3,5-Dihydroxybenzoic acid methyl ester is a potent tyrosinase inhibitor that has been shown to be effective in inhibiting the production of melanin. 3,5-Dihydroxybenzoic acid methyl ester is an active ingredient in skin lightening products and has been shown to be more potent than kojic acid, arbutin and ascorbic acid. The reaction mechanism of 3,5-Dihydroxybenzoic acid methyl ester is stepwise with hydroxybenzoic acid (HBA) being the first substrate. HBA reacts with iron oxides to form a ferric hydroxide intermediate that undergoes gelation reactions with chloride ions. This results in a molecule containing three ether linkages, which are responsible for its inhibitory activity on the enzyme tyrosinase.

Formula: C₈H₈O₄

Purity: Min. 95%

Color and Shape: Powder

Molecular weight: 168.15 g/mol

Ref: 3D-FD22105