5-Methylsalicylic Acid TCI C0410

Chemical Identity

Other names: p-Cresotic Acid · 2-Hydroxy-5-methylbenzoic Acid · 6-Hydroxy-m-toluic Acid
CAS No.: 89-56-5
PubChem: CID 6973·SID 87565537
Formula: C8H8O3
Molecular weight: 152.15 g/mol
Purity: >98.0%(T)
Reference databases: ChemSpider·ECHA·Wikipedia

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: 2-hydroxy-5-methylbenzoic acid
SMILES: CC1=CC(=C(C=C1)O)C(=O)O
InChIKey: DLGBEGBHXSAQOC-UHFFFAOYSA-N
MDL: MDL00002461

Rp 955.500,00

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Berat 5g 25g

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TCI C0410 5-Methylsalicylic Acid (CAS 89-56-5) is a methyl-substituted salicylic acid derivative intended for research-scale synthesis and coordination chemistry. Its ortho-hydroxybenzoic acid core offers predictable reactivity for preparing esters, amides, and metal complexes. AMI Scientific supplies this TCI product in 5 g and 25 g packs, sizes well suited to exploratory or micro-scale reactions. Store it in a cool, dry place in a tightly sealed container and review the Safety Data Sheet before use.

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Spencer et al. (1990). Use of chiral malonates to determine the absolute configuration of the hydrogen atoms eliminated during the formation of 6-methylsalicylic acid by 6-methylsalicylic acid synthase from Penicillium patulum. Journal of the Chemical Society, Chemical Communications doi:10.1039/c39900001704
Spencer et al. (1992). Purification and properties of 6-methylsalicylic acid synthase from Penicillium patulum. Biochemical Journal doi:10.1042/bj2880839
Yalpani (2001). Production of 6-Methylsalicylic Acid by Expression of a Fungal Polyketide Synthase Activates Disease Resistance in Tobacco. THE PLANT CELL ONLINE doi:10.1105/tpc.13.6.1401

References were compiled automatically from Crossref and every DOI was verified to exist. AMI Scientific is not affiliated with the authors or the publishers.