D108405
3,4-Dihydroxybenzaldehyde
97%
Synonym(s):
Protocatechualdehyde
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About This Item
Linear Formula:
(HO)2C6H3CHO
CAS Number:
Molecular Weight:
138.12
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
205-377-7
Beilstein/REAXYS Number:
774381
MDL number:
Assay:
97%
Form:
powder
Quality Level
assay
97%
form
powder
mp
150-157 °C (lit.)
SMILES string
Oc1ccc(C=O)cc1O
InChI
1S/C7H6O3/c8-4-5-1-2-6(9)7(10)3-5/h1-4,9-10H
InChI key
IBGBGRVKPALMCQ-UHFFFAOYSA-N
Application
3,4-Dihydroxybenzaldehyde can be used as a reactant for the synthesis of:
- Copolymers containing poly(p-phenylenevinylene) chromophore to be used in light-emitting electrochemical cell.
- 2-Arylbenzothiazoles with potential application as anti-cancer agents against human colon cancer cells.
- Variety of thiazolidin-4-one ring systems having antimicrobial activity.
- Bis-Schiff bases of isatins which can be used as antiglycating agents.
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signalword
Warning
hcodes
Hazard Classifications
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
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Synthesis of new bioactive venlafaxine analogs: Novel thiazolidin-4-ones as antimicrobials.
Kavitha CV, et al.
Bioorganic & Medicinal Chemistry, 14(7), 2290-2299 (2006)
Synthesis and electroluminescence of novel copolymers containing crown ether spacers.
Sun Q, et al.
Journal of Materials Chemistry, 13(4), 800-806 (2003)
Synthesis of bis-Schiff bases of isatins and their antiglycation activity.
Khan KM, et al.
Bioorganic & Medicinal Chemistry, 17(22), 7795-7801 (2009)