H16205
Homophthalic acid
98%
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
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
201-913-9
Beilstein/REAXYS Number:
1872069
MDL number:
Assay:
98%
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
Other Notes
Remainder phthalic acid
Storage Class
11 - 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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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
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
Global Trade Item Number
| SKU | GTIN |
|---|---|
| H16205-25G | 04061831826890 |
| H16205-100G | 04061833670354 |