I19209
Isophthalic acid
99%
Synonym(s):
Benzene-1,3-dicarboxylic acid
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500 G
$43.74
2 KG
$102.00
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500 G
$43.74
2 KG
$102.00
About This Item
Linear Formula:
C6H4-1,3-(CO2H)2
CAS Number:
Molecular Weight:
166.13
Beilstein/REAXYS Number:
1909332
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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Quality Level
assay
99%
autoignition temp.
1198 °F
mp
341-343 °C (lit.)
SMILES string
OC(=O)c1cccc(c1)C(O)=O
InChI
1S/C8H6O4/c9-7(10)5-2-1-3-6(4-5)8(11)12/h1-4H,(H,9,10)(H,11,12)
Inchi Key
QQVIHTHCMHWDBS-UHFFFAOYSA-N
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Application
Isophthalic acid can be used as a reactant to prepare:
It can also be used as a ligand to synthesize:
- Poly(m-phenyleneisophthalamide) by polycondensation with m-phenylenediamine via thermal solid-phase polymerization reaction.[1]
It can also be used as a ligand to synthesize:
- Metal coordination polymers by hydrothermal and sonochemical process.[2]
- Isophthalic acid-zirconium(IV) nanocomposite, which is used as a precursor to prepare crystalline tetragonal ZrO2 via thermal decomposition method.[3]
Storage Class
13 - Non Combustible Solids
wgk_germany
WGK 2
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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Self-assembly of organic molecules at solid-liquid interfaces is a route for developing novel functional materials on surfaces and modeling assembly phenomena in 3D. 5-Alkoxylated isophthalic acids (ISA) are known to self-assemble into two-dimensional (2D) lamellae at the interface between a
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We have identified small-molecule dibenzazepine inhibitors of beta-secretase (BACE1). These BACE1 inhibitors possess two key salient features. The first is a seven-membered heterocyclic ring fused to two aromatic rings representing the P3-P2 residues. The second is an amide and/or amide
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