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Merck
CN

47733

5-Formylsalicylic acid

purum, ≥95.0% (T)

Synonym(s):

2-Hydroxy-5-formylbenzoic acid

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About This Item

Linear Formula:
HCOC6H3-2-(OH)CO2H
CAS Number:
Molecular Weight:
166.13
EC Number:
210-492-0
UNSPSC Code:
12352100
PubChem Substance ID:
Beilstein/REAXYS Number:
2640881
MDL number:
Assay:
≥95.0% (T)
Form:
powder
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InChI key

UTCFOFWMEPQCSR-UHFFFAOYSA-N

InChI

1S/C8H6O4/c9-4-5-1-2-7(10)6(3-5)8(11)12/h1-4,10H,(H,11,12)

SMILES string

OC(=O)c1cc(C=O)ccc1O

grade

purum

assay

≥95.0% (T)

form

powder

color

brownish-yellow

mp

250 °C (dec.) (lit.)

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General description

5-Formylsalicylic acid (5-FSA) is a derivative salicylic acid. It participates in the formation of chelation ion exchange resins. The reaction of 5-FPA with activated methylene compounds has been studied.

Application

5-Formylsalicylic acid may be used in the synthesis of 5-(benzimidazolium-2-yl)salicylate by reacting with o-phenylene­diamine.

pictograms

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Warning

Hazard Classifications

Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - Skin Sens. 1

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

Regulatory Information

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Metal Uptake Properties of Polystyrene Resin Immobilized Polyamine and Formylsalicylic Acid Derivatives as Chelation Ion Exchangers.
Mahmoud ME, et al.
Analytical Sciences, 13(5), 765-769 (1997)
Cinnamoylnitrile-, pyran-, and pyranopyrazole-derivatives containing the salicylanilide moiety with anticipated molluscicidal activity.
Nawwar GAM, et al.
Arch. Pharm. (Weinheim), 324(11), 875-877 (1991)
5-Formylsalicylic acid and 5-(benzimidazolium-2-yl) salicylate.
Lu YB, et al.
Acta Crystallographica Section C, Structural Chemistry, 66(12), o596-o599 (2010)
Manabu Nakazono et al.
Clinica chimica acta; international journal of clinical chemistry, 436, 27-34 (2014-05-13)
Various styrylbenzene compounds were synthesized and evaluated as mainly Aβ amyloid sensors. These compounds, however, cannot be used for detecting amyloid deposition in peripheral nerves because of the inherent sensitivity of the compounds. These compounds often generate false positives especially

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