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Merck
CN

152153

2-甲酰苯氧乙酸

97%

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关于此项目

线性分子式:
HCOC6H4OCH2CO2H
化学文摘社编号:
分子量:
180.16
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
228-480-9
MDL number:
Assay:
97%
Form:
solid
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assay

97%

form

solid

mp

129.5-132 °C (lit.)

functional group

aldehyde, carboxylic acid

SMILES string

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 key

ANWMNLAAFDCKMT-UHFFFAOYSA-N

Application

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


存储类别

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)



历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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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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货号GTIN
152153-25G04061838740236