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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
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Assay
97%
form
solid
mp
145-147 °C (lit.)
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 Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Certificates of Analysis (COA)
Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.
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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)
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)
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