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About This Item
Linear Formula:
ClC6H3(OH)CHO
CAS Number:
Molecular Weight:
156.57
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
assay
97%
form
solid
mp
145-147 °C (lit.)
functional group
aldehyde
chloro
SMILES string
Oc1ccc(C=O)c(Cl)c1
InChI
1S/C7H5ClO2/c8-7-3-6(10)2-1-5(7)4-9/h1-4,10H
InChI key
ZMOMCILMBYEGLD-UHFFFAOYSA-N
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General description
N-Thioamide thiosemicarbazone derivatives of 2-chloro-4-hydroxy-benzaldehyde have been prepared. pK values for acid dissociation of 2-chloro-4-hydroxybenzaldehyde has been evaluated.
Application
2-Chloro-4-hydroxybenzaldehyde may be used in chemical synthesis.
Storage Class
11 - Combustible Solids
wgk_germany
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
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Synthesis and characterization of thiosemicarbazone derivatives of 2-chloro-4-hydroxy-benzaldehyde and their rhenium (I) complexes.
Nu?ez-Montenegro A, et al.
Polyhedron, 28(18), 3915-3922 (2009)
Coordination in Solutions. II. Acid Dissociation Constants in Water and Structural Reassignments of the Isomeric Chlorosalicylaldehydes1, 2.
Postmus Jr C, et al.
The Journal of Organic Chemistry, 29(9), 2693-2698 (1964)
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