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Merck
CN

53580

邻羧基苯乙酸

purum, ≥99.0% (HPLC)

别名:

α-羧基邻甲苯酸, 2-羧基苯乙酸

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线性分子式:
HO2CCH2C6H4CO2H
化学文摘社编号:
分子量:
180.16
EC Number:
201-913-9
UNSPSC Code:
12352100
PubChem Substance ID:
Beilstein/REAXYS Number:
1872069
MDL number:
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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

存储类别

13 - Non Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

法规信息

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分析证书(COA)

Lot/Batch Number

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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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