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About This Item
Linear Formula:
ClC6H3(OH)CHO
CAS Number:
Molecular Weight:
156.57
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
211-244-4
MDL number:
Product Name
5-Chlorosalicylaldehyde, 98%
InChI key
FUGKCSRLAQKUHG-UHFFFAOYSA-N
InChI
1S/C7H5ClO2/c8-6-1-2-7(10)5(3-6)4-9/h1-4,10H
SMILES string
Oc1ccc(Cl)cc1C=O
assay
98%
form
solid
mp
100-102 °C (lit.)
functional group
aldehyde
chloro
Quality Level
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signalword
Warning
hcodes
Hazard Classifications
Aquatic Acute 1 - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
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Govindan Prakash et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 129, 352-358 (2014-04-22)
Schiff base disulfide ligands (H2L(1-6)) were synthesized from the condensation of cystamine with salicylaldehyde(H2L(1)), 5-chlorosalicylaldehyde(H2L(2)), o-vanillin(H2L(3)), 2-hydroxyacetophenone(H2L(4)), 3-methyl-2-hydroxyacetophenone(H2L(5)), and 2-hydroxy-1-naphthaldehyde(H2L(6)). H2L(1-6) reacts with the ruthenium precursor complex [RuHCl(CO)(PPh3)3] in benzene giving rise to six new ruthenium(II) complexes of general formula
Shipra Sagar et al.
Dalton transactions (Cambridge, England : 2003), 46(4), 1249-1259 (2017-01-07)
In the present work, two new copper complexes 3a and 3b with a Cu
Verónica Ferraresi-Curotto et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 137, 692-700 (2014-09-26)
Five Schiff bases obtained from condensation of 4-methoxybenzohydrazide with related aldehydes, namely o-vanillin, vanillin, 5-bromovanillin, 5-chlorosalicylaldehyde and 5-bromosalicylaldehyde were prepared. A detailed structural and spectroscopic study is reported. The crystal structures of four members of the family were determined and
Xiaotong Chen et al.
Analytica chimica acta, 625(1), 41-46 (2008-08-30)
A facile fluorescent method for the determination of hydrazine in aqueous solution with excellent sensitivity was developed. 5-chlorosalicylaldehyde (CS), a readily commercially available compound, was applied as the derivatization reagent in this work. Under the addition of CS to hydrazine
Kanalli V Ajeya et al.
Journal of hazardous materials, 399, 123047-123047 (2020-09-18)
To recover the spent vanadium compound, Rhodamine-B-based Schiff's base ligand (L1) was synthesized via ultrasonication process and was evaluated with vanadyl sulfate (VOSO4), which has shown considerable selectivity towards V(IV). The change of the solution color from colorless to pink
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