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| 4-Pyridinecarboxaldehyde Chemical Properties |
Melting point | -4--2°C | Boiling point | 71-73 °C/10 mmHg (lit.) | density | 1.137 g/mL at 20 °C (lit.) | vapor pressure | 0.02 hPa (20 °C) | refractive index | n20/D 1.544(lit.) | Fp | 130 °F | storage temp. | Store at +2°C to +8°C. | solubility | 20g/l | pka | 12.05(at 30℃) | form | liquid (clear) | color | clear brown-yellow | PH | 7-8 (H2O, 20℃)(saturated aqueous solution) | Water Solubility | 20 g/L (20 ºC) | Sensitive | Air Sensitive | BRN | 105342 | InChIKey | BGUWFUQJCDRPTL-UHFFFAOYSA-N | LogP | 0.12 at 30℃ and pH7 | CAS DataBase Reference | 872-85-5(CAS DataBase Reference) | NIST Chemistry Reference | 4-Pyridinecarboxaldehyde(872-85-5) | EPA Substance Registry System | 4-Pyridinecarboxaldehyde (872-85-5) |
Hazard Codes | Xi,F | Risk Statements | 36/37/38-10 | Safety Statements | 26-36-36/37/39-16 | RIDADR | UN 1989 | WGK Germany | 1 | RTECS | NR9400000 | F | 8-10-23 | Hazard Note | Irritant/Keep Cold/Air Sensitive | TSCA | Yes | HazardClass | 3.2 | PackingGroup | III | HS Code | 29333999 | Toxicity | LD50 orally in Rabbit: 2355 mg/kg LD50 dermal Rat > 2000 mg/kg |
| 4-Pyridinecarboxaldehyde Usage And Synthesis |
Flavor Type | Flavor Type: fruity
| Chemical Properties | 4-Pyridinecarboxaldehyde(4PCA) is a slightly yellow oily liquid. Its relative density is 1.122, and its refractive index is 1.5352 (25°C). Flash point is 54 ° C. 4-Pyridinecarboxaldehyde is soluble in water and ether.4-Pyridinecarboxaldehyde, also commonly called pyridine-2-carboxaldehyde, is an organic compound with the formula NC5H4CHO. 4-Pyridinecarboxaldehyde is a colorless oily liquid with a distinctive odor. Older samples are often brown-colored owing to impurities.
| Uses | 4-Pyridinecarboxaldehyde is an heterocyclic building block used for the synthesis of various pharmaceutical compounds, such as new 1,4-dihydropyridin-4-yl-phenoxyacetohydrazones, having anticonvulsant and anti-inflammatory properties.4-Pyridinecarboxaldehyde and some of its derivatives have also been reported as useful transamination reagents to introduce ketone or aldehyde groups onto the N-termini of antibodies for subsequent site-specifically conjugate aminooxy-functionalized molecules (including fluorescent dyes, polyethylene glycol, or porphyrins) to these entities.
4-Pyridinecarboxaldehyde can be used for the synthesis of: 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.
| Chemical Properties | clear yellow-brown liquid. soluble in water and ether. | Uses | 4-Pyridinecarboxaldehyde can be used for the synthesis of:
- ?,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.
| Uses | 4-Pyridinecarboxaldehyde, is an heterocyclic building block used for the synthesis of various pharmaceutical compounds, such as new 1,4-dihydropyridin-4-yl-phenoxyacetohydrazones, having anticonvulsant and anti-inflammatory properties. | Preparation | 4-Pyridinecarbaldehyde is synthesized by oxidation of 4-picoline. The mixed gas of 4-picoline and air is passed through the vanadium-molybdenum catalyst layer heated to 400°C, and oxidized to generate 4-pyridinecarbaldehyde. | Synthesis Reference(s) | Synthetic Communications, 20, p. 3385, 1990 DOI: 10.1080/00397919008051576 | Purification Methods | Purified as for pyridine-2-aldehyde. [Beilstein 21 III/IV 2529, 21/7 V 351.] |
| 4-Pyridinecarboxaldehyde Preparation Products And Raw materials |
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