53580
Homophthalic acid
purum, ≥99.0% (HPLC)
Synonym(s):
α-Carboxy-o-toluic acid, 2-Carboxyphenylacetic acid
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About This Item
Linear Formula:
HO2CCH2C6H4CO2H
CAS Number:
Molecular Weight:
180.16
EC Number:
201-913-9
UNSPSC Code:
12352100
PubChem Substance ID:
Beilstein/REAXYS Number:
1872069
MDL number:
grade
purum
assay
≥99.0% (HPLC)
ign. residue
≤0.1%
mp
178-182 °C (lit.), 180-182 °C
SMILES string
OC(=O)Cc1ccccc1C(O)=O
InChI
1S/C9H8O4/c10-8(11)5-6-3-1-2-4-7(6)9(12)13/h1-4H,5H2,(H,10,11)(H,12,13)
InChI key
ZHQLTKAVLJKSKR-UHFFFAOYSA-N
Storage Class
13 - Non Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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T B Karegoudar et al.
FEMS microbiology letters, 49(2-3), 305-308 (1989-04-01)
A microorganism capable of degrading homophthalic acid as a sole source of carbon was isolated from soil. The strain was tentatively identified as Pseudomonas sp. Oxygen uptake studies were carried out with possible intermediates. Assays for several different enzymes were
Khalid Mohammed Khan et al.
Natural product research, 22(13), 1120-1127 (2008-10-16)
A microwave-assisted, environmentally friendly, high-yielding, time-saving synthesis of medicinally important 3-substituted isocoumarins was carried out in a single step by direct condensation of homophthalic acid with aryol and acyl chlorides under solvent-free conditions without any solid support. The synthesised isocoumarins
C S Karigar et al.
FEMS microbiology letters, 110(1), 59-64 (1993-06-01)
A microorganism capable of degrading homophthalic acid as a sole carbon source was isolated from garden soil. The strain was identified as Pseudomonas alcaligenes. The organism degraded homophthalate by a pathway which involved phenylacetate and p-hydroxyphenylacetate as intermediates. The intermediates
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