H16205
Homophthalic acid
98%
Sinônimo(s):
α-Carboxy-o-toluic acid, 2-Carboxyphenylacetic acid
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About This Item
Produtos recomendados
Nível de qualidade
Ensaio
98%
pf
178-182 °C (lit.)
cadeia de caracteres SMILES
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)
chave InChI
ZHQLTKAVLJKSKR-UHFFFAOYSA-N
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Outras notas
Remainder phthalic acid
Código de classe de armazenamento
11 - Combustible Solids
Classe de risco de água (WGK)
WGK 3
Ponto de fulgor (°F)
Not applicable
Ponto de fulgor (°C)
Not applicable
Equipamento de proteção individual
Eyeshields, Gloves, type N95 (US)
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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
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
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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