H16205
Homophthalic acid
98%
Synonym(s):
α-Carboxy-o-toluic acid, 2-Carboxyphenylacetic acid
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All Photos(2)
About This Item
Linear Formula:
HO2CCH2C6H4CO2H
CAS Number:
Molecular Weight:
180.16
Beilstein:
1872069
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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Assay
98%
mp
178-182 °C (lit.)
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
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Other Notes
Remainder phthalic acid
Storage Class Code
11 - 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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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
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
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
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