| Weight | 168.148 g/mol |
|---|---|
| Formula | C8H8O4 |
| Hydrogen Acceptors | 4 |
| Hydrogen Donors | 2 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 1 |
Methyl 2,5-dihydroxybenzoate (2150-46-1)
methyl gentisate
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- Allergic contact dermatitis from methyl gentisate in a bleaching cream (Contact Dermatitis, 2006)
- Synthesis of functionalized para -and meta -terphenyls based on site-selective Suzuki cross-coupling reactions of bis(triflates) of methyl 2,5-dihydroxybenzoate and methyl 2,4-dihydroxybenzoate (Canadian Journal of Chemistry, 2012)
- Un nouvel exemple de driv nitr d'origine naturelle: Le nitro-3 mthyl-5 gentisate de mthyle, extrait des racines de Primula acaulis (Phytochemistry, 1971)
- Allergic contact dermatitis to methyl gentisate (Contact Dermatitis, 2009)
- Methyl 2,5-dihydroxybenzoate (Acta Crystallographica Section E-structure Reports Online, 2003)
- ChemInform Abstract: Synthesis of Functionalized para and metaTerphenyls Based on SiteSelective Suzuki CrossCoupling Reactions of Bis(triflates) of Methyl 2,5Dihydroxybenzoate and Methyl 2,4Dihydroxybenzoate. (ChemInform, 2014)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - methyl gentisate
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SMILESCOC(=O)C1=C(C=CC(=C1)O)O
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InChIKeyXGDPKUKRQHHZTH-UHFFFAOYSA-N
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Similar Compounds
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