All Photos(3)
About This Item
Linear Formula:
Cl2C6H3CHO
CAS Number:
Molecular Weight:
175.01
Beilstein/REAXYS Number:
471601
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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Quality Level
assay
99%
form
solid
bp
233 °C (lit.)
mp
64-69 °C (lit.)
functional group
aldehyde
chloro
SMILES string
[H]C(=O)c1ccc(Cl)cc1Cl
InChI
1S/C7H4Cl2O/c8-6-2-1-5(4-10)7(9)3-6/h1-4H
InChI key
YSFBEAASFUWWHU-UHFFFAOYSA-N
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General description
2,4-Dichlorobenzaldehyde on condensation with 4-amino-5-mercapto-3-methyl/ethyl-1,2,4-triazole yields bidentate Schiff base ligands and their metal complexes are potential antimicrobial agents.
Application
2,4-Dichlorobenzaldehyde was used in the solid-phase synthesis of a series of indole-based peptoids.
signalword
Danger
hcodes
Hazard Classifications
Aquatic Chronic 2 - Eye Dam. 1 - Skin Corr. 1B
Storage Class
8A - Combustible corrosive hazardous materials
wgk_germany
WGK 2
flash_point_f
275.0 °F - closed cup
flash_point_c
135 °C - closed cup
ppe
Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
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A series of cobalt, nickel, copper, and zinc complexes of bidentate Schiff bases derived from the condensation reaction of 4-amino-5-mercapto-3-methyl/ethyl-1,2,4-triazole with 2,4-dichlorobenzaldehyde were synthesized and tested as antimicrobial agents. The synthesized Schiff bases and their metal complexes were characterized with
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