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About This Item
Empirical Formula (Hill Notation):
C6H5NO
CAS Number:
Molecular Weight:
107.11
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
212-832-3
Beilstein/REAXYS Number:
105342
MDL number:
Assay:
97%
Quality Level
assay
97%
refractive index
n20/D 1.544 (lit.)
bp
71-73 °C/10 mmHg (lit.)
density
1.137 g/mL at 20 °C (lit.)
storage temp.
2-8°C
SMILES string
[H]C(=O)c1ccncc1
InChI
1S/C6H5NO/c8-5-6-1-3-7-4-2-6/h1-5H
InChI key
BGUWFUQJCDRPTL-UHFFFAOYSA-N
General description
4-Pyridinecarboxaldehyde is a heterocyclic building block used to prepare Schiff bases via a Korich-type reaction.
Application
4-Pyridinecarboxaldehyde can be used for the synthesis of:
- ʅ,β-Unsaturated amides by coupling with N,N-disubstituted formamides.
- meso-Substituted A3-corroles.
- N-(4-pyridylmethyl)-L-valine as a ligand to construct zinc metal–organic frameworks (Zn-MOFs).
- 4′-Pyridyl terpyridines, with potential application as anticancer and antimicrobial agents.
- 4-pyridinecarboxaldehyde thiosemicarbazone, as a corrosion inhibitor for mild steel.
signalword
Danger
hcodes
Hazard Classifications
Aquatic Chronic 3 - Eye Dam. 1 - Skin Corr. 1B - Skin Sens. 1
Storage Class
8A - Combustible corrosive hazardous materials
wgk
WGK 1
flash_point_f
172.0 °F
flash_point_c
77.8 °C
ppe
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
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Experimental and theoretical evaluation of two pyridinecarboxaldehyde thiosemicarbazone compounds as corrosion inhibitors for mild steel in hydrochloric acid solution.
Xu B, et al.
Corrosion Science, 78(9), 260-268 (2014)
Poly (ethyleneglycol)(PEG): a versatile reaction medium in gaining access to 4?-(pyridyl)-terpyridines.
Smith CB, et al.
Green Chemistry, 7(9), 650-654 (2005)
Efficient synthesis of meso-substituted corroles in a H2O- MeOH mixture.
Koszarna B and Gryko DT
The Journal of Organic Chemistry, 71(10), 3707-3717 (2006)
Global Trade Item Number
| SKU | GTIN |
|---|---|
| P62402-25G | 04061834393122 |
| P62402-500G | 04061838137319 |
| P62402-100G | 04061834393115 |

