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About This Item
Linear Formula:
CH3OC6H3(CH3)CO2H
CAS Number:
Molecular Weight:
166.17
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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Assay
97%
mp
177-181 °C (lit.)
functional group
carboxylic acid
SMILES string
COc1ccc(C(O)=O)c(C)c1
InChI
1S/C9H10O3/c1-6-5-7(12-2)3-4-8(6)9(10)11/h3-5H,1-2H3,(H,10,11)
InChI key
MSVRGYOYISBGTH-UHFFFAOYSA-N
General description
4-Methoxy-2-methylbenzoic acid (2-methylanisic acid) is a trisubstituted aromatic compound. It is a positional isomeric form of 2-methoxy-4-methylbenzoic acid. 4-Methoxy-2-methylbenzoic acid readily forms complexes with Mn(II), Co(II), Ni(II), Cu(II), Zn(II) and Cd(II).
Application
4-Methoxy-2-methylbenzoic acid may be used in the synthesis of 4-methoxy-2-methylbenzoates of Y(III) and lanthanides (III) (La to Lu, excluding Pm). It may also be used to synthesize 4-methoxy-2-methylbenzoic acid hydrazide and 5-bromo-4-methoxy-2-methylbenzoic acid.
Storage Class Code
13 - Non Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
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Spectral and thermal investigation of rare earth element 4-methoxy-2-methylbenzoates.
Brzyska W and Ozga W.
Journal of Thermal Analysis and Calorimetry, 70(2), 467-474 (2002)
A Omodei-Salé et al.
Journal of medicinal chemistry, 26(8), 1187-1192 (1983-08-01)
A series of 3,5-diaryl-s-triazoles were synthesized and evaluated as postimplantation contragestational agents. The introduction of various substituents (e.g., an o-alkyl chain on one phenyl and a m-alkoxy group on the other) was found to increase the potency. Several compounds with
Thermal, spectral and magnetic investigations of Mn (II), Co (II), Ni (II), Cu (II), Zn (II) and cd (ii) complexes with 4-methoxy-2-methylbenzoic acid.
Meganathan C, et al.
Polish Journal of Chemistry, 76(12), 1689-1692 (2002)
Peng Hu et al.
Organic letters, 11(11), 2341-2344 (2009-05-13)
A versatile palladium catalyst system was developed to effect the decarboxylative Heck coupling of a variety of arenecarboxylic acids with a wide range of olefins. The key to obtaining the efficient catalyst system is the use of 1-adamatanecarboxylic acid as
(1 S)-1, 5-Anhydro-1-[5-(4-ethoxybenzyl)-2-methoxy-4-methylphenyl]-1-thio-d-glucitol (TS-071) is a potent, selective sodium-dependent glucose cotransporter 2 (SGLT2) inhibitor for type 2 diabetes treatment.
Kakinuma H, et al.
Journal of Medicinal Chemistry, 58(3), 3247- 3261 (2010)
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