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重要文件

152153

Sigma-Aldrich

2-甲酰苯氧乙酸

97%

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About This Item

線性公式:
HCOC6H4OCH2CO2H
CAS號碼:
分子量::
180.16
EC號碼:
MDL號碼:
分類程式碼代碼:
12352100
PubChem物質ID:
NACRES:
NA.22
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化驗

97%

形狀

solid

mp

129.5-132 °C (lit.)

官能基

aldehyde
carboxylic acid

SMILES 字串

OC(=O)COc1ccccc1C=O

InChI

1S/C9H8O4/c10-5-7-3-1-2-4-8(7)13-6-9(11)12/h1-5H,6H2,(H,11,12)

InChI 密鑰

ANWMNLAAFDCKMT-UHFFFAOYSA-N

應用

2-Formylphenoxyacetic acid was used to synthesize azomethine derivatives[1]. It was also used in the preparation of ligands L(1)H(2) and L(2)H(2)[2].

儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

WGK 3

閃點(°F)

Not applicable

閃點(°C)

Not applicable

個人防護裝備

Eyeshields, Gloves, type N95 (US)


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Priya P Netalkar et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 97, 762-770 (2012-08-21)
A series of novel Co(II), Ni(II), Cu(II) and Zn(II) complexes of tri and tetratopic hydrazones have been prepared. Ligands L(1)H(2) and L(2)H(2) were synthesized by the condensation of 2-formylphenoxyacetic acid with 2-hydrazinobenzothiazole and 2-hydroxy-3-hydrazinebenzopyrazine, respectively. The prepared complexes were characterized
Amjid Iqbal et al.
Molecules (Basel, Switzerland), 12(2), 245-254 (2007-09-12)
A series of eight new azomethine derivatives were synthesized by reacting 2-formylphenoxyacetic acid with aromatic amines. The chemical structures of these compounds were confirmed by means of 1H-NMR, 13C-NMR, MS and elemental analysis. The compounds were assayed by the disc

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