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TCI

CAS 83-40-9

3-Methylsalicylic Acid TCI C0408

3-Methylsalicylic Acid TCI C0408

Chemical Identity

Other names
o-Cresotic Acid · 2-Hydroxy-3-methylbenzoic Acid · 2-Hydroxy-m-toluic Acid
CAS No.
83-40-9
PubChem
CID 6738·SID 87565535
Formula
C8H8O3
Molecular weight
152.15 g/mol
Purity
>98.0%(GC)(T)
Reference databases
ChEBI·ChemSpider·ECHA·Wikipedia
Full identifiers (IUPAC, SMILES, InChIKey)
IUPAC
2-hydroxy-3-methylbenzoic acid
SMILES
CC1=C(C(=CC=C1)C(=O)O)O
InChIKey
WHSXTWFYRGOBGO-UHFFFAOYSA-N
MDL
MDL00002448
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TCI C0408 3-Methylsalicylic Acid (CAS 83-40-9) is a methyl-substituted salicylic acid derivative supplied as a non-heterocyclic building block for laboratory synthesis. Its phenolic hydroxyl and carboxylic acid groups provide two selectively addressable reaction sites, making it useful in multi-step organic chemistry and coordination studies. AMI Scientific offers this TCI catalogue item in 25 g, 100 g, and 500 g pack sizes to suit different working scales. Store the material in a cool, dry, well-ventilated area in a tightly closed container, and always consult the manufacturer's Safety Data Sheet before handling.

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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
  • Snini et al. (2014). The gene PatG involved in the biosynthesis pathway of patulin, a food-borne mycotoxin, encodes a 6-methylsalicylic acid decarboxylase. International Journal of Food Microbiology doi:10.1016/j.ijfoodmicro.2013.11.020

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