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About This Item
Linear Formula:
BrC6H3-2-(OH)CHO
CAS Number:
Molecular Weight:
201.02
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
217-167-2
Beilstein/REAXYS Number:
774710
MDL number:
Assay:
98%
Form:
powder
Quality Segment
assay
98%
form
powder
mp
102-106 °C (lit.)
functional group
aldehyde, bromo
SMILES string
Oc1ccc(Br)cc1C=O
InChI
1S/C7H5BrO2/c8-6-1-2-7(10)5(3-6)4-9/h1-4,10H
InChI key
MKKSTJKBKNCMRV-UHFFFAOYSA-N
General description
5-Bromosalicylaldehyde reacts with 1,2-bis(4-chloro-2-aminophenoxy)ethane to yield Schiff base ligand 1,2-bis(2-(5-bromo-2-hydroxybenzilidenamino)-4-chlorophenoxy)ethane. It is the starting reagent for the synthesis of diarylamino-substituted N-methyl tetrahydrosalen ligand.
5-Bromosalicylaldehyde is generally used to synthesize schiff bases, and triphenyltin complexes.
5-Bromosalicylaldehyde is generally used to synthesize schiff bases, and triphenyltin complexes.
Application
5-Bromosalicylaldehyde was used for chemical derivatization during amine quantiifcation in poly (ethylene terephthalate) (PET) film and PET scaffold.
Storage Class
11 - Combustible Solids
ppe
dust mask type N95 (US), Eyeshields, Gloves
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Aquatic Chronic 2 - Skin Irrit. 2 - Skin Sens. 1B
signalword
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