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Thermo Scientific Chemicals
Methyl 2,4-dihydroxybenzoate, 97%
CAS: 2150-47-2 | C8H8O4 | 168.148 g/mol
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Catalog number B24757.22
also known as B24757-22
Price (USD)
101.65
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113.00Save 11.35 (10%)
Each
Quantity:
100 g
Price (USD)
101.65
Online Exclusive
113.00Save 11.35 (10%)
Each
Chemical Identifiers
CAS2150-47-2
IUPAC Namemethyl 2,4-dihydroxybenzoate
Molecular FormulaC8H8O4
InChI KeyIIFCLXHRIYTHPV-UHFFFAOYSA-N
SMILESCOC(=O)C1=CC=C(O)C=C1O
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Specifications
Specification Sheet
Specification SheetAppearance (Color)Pale cream
Melting Point (clear melt)113.0-122.0?C
FormCrystals or powder or crystalline powder
Assay (GC)≥96.0%
Methyl 2,4-dihydroxybenzoate is used as a cosmetic agents. And it is used in synthesis of raw material for fine chemicals, organic intermediate, pharmaceutical intermediate.
This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.
Applications
Methyl 2,4-dihydroxybenzoate is used as a cosmetic agents. And it is used in synthesis of raw material for fine chemicals, organic intermediate, pharmaceutical intermediate.
Solubility
Soluble in methanol.
Notes
Keep container tightly closed. Store away from oxidizing agents.
Methyl 2,4-dihydroxybenzoate is used as a cosmetic agents. And it is used in synthesis of raw material for fine chemicals, organic intermediate, pharmaceutical intermediate.
Solubility
Soluble in methanol.
Notes
Keep container tightly closed. Store away from oxidizing agents.
RUO – Research Use Only
General References:
- Osamu Fujimura.; Gregory C. Fu.; Robert H. Grubbs. The Synthesis of Cyclic Enol Ethers via Molybdenum Alkylidene-Catalyzed Ring-Closing Metathesis. J. Org. Chem. 1994, 59, (15), 4029-4031.
- Hiroyuki Saimoto.; Koji Yoshida.; Tetsuya Murakami.; Minoru Morimoto.; Hitoshi Sashiwa.; Yoshihiro Shigemasa. Effect of Calcium Reagents on Aldol Reactions of Phenolic Enolates with Aldehydes in Alcohol. J. Org. Chem. 1996, 61, (20), 6768-6769.