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About This Item
Linear Formula:
CH3OC6H3(CO2H)2
CAS Number:
Molecular Weight:
196.16
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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Assay
97%
mp
258-263 °C (lit.)
SMILES string
COc1ccc(cc1C(O)=O)C(O)=O
InChI
1S/C9H8O5/c1-14-7-3-2-5(8(10)11)4-6(7)9(12)13/h2-4H,1H3,(H,10,11)(H,12,13)
InChI key
JIICYHFLIOGGHE-UHFFFAOYSA-N
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General description
4-Methoxyisophthalic acid can be prepared by employing the following as a starting material:
- its dimethyl analog
- p-cresol
- 4-methoxy-m-xylene
- 3-methyl-4-methoxybenzyl chloride
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
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Some Normal and Alkamine Esters of 4-Methoxyisophthalic Acid.
Fosdick LS and Fancher OE.
Journal of the American Chemical Society, 63(5), 1277-1279 (1941)
Poly (Benzimidazole) synthesis by direct reaction of methoxyphthalic acids and tetramine.
Ueda M and Sugita H.
Journal of Polymer Science Part A: Polymer Chemistry, 27(8), 2815-2818 (1989)
Hydroxyphenylisopropylamines containing nuclear methyl groups.
Wenner W.
The Journal of Organic Chemistry, 16(3), 457-460 (1951)
Structure determination and synthesis of a plant growth inhibitor, 3-acetyl-6-methoxybenzaldehyde, found in the leaves of Encelia farinosa.
R GRAY et al.
Journal of the American Chemical Society, 70(3), 1249-1253 (1948-03-01)
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