Cas no 87883-20-3 (5-nitro-3-Pyridinecarboxaldehyde)

5-nitro-3-Pyridinecarboxaldehyde is a versatile compound with significant applications in organic synthesis. It offers high purity and stability, enabling efficient reactions with various nucleophiles. This compound's distinct nitro group facilitates selective transformations, enhancing synthetic yield and purity. Its unique structure and reactivity make it a valuable building block in the synthesis of complex organic molecules.
5-nitro-3-Pyridinecarboxaldehyde structure
87883-20-3 structure
Product Name:5-nitro-3-Pyridinecarboxaldehyde
CAS No:87883-20-3
MF:C6H4N2O3
MW:152.10756111145
CID:651153
Update Time:2025-06-25

5-nitro-3-Pyridinecarboxaldehyde Chemical and Physical Properties

Names and Identifiers

    • 5-nitro-3-Pyridinecarboxaldehyde
    • 3-Pyridinecarboxaldehyde, 5-nitro-
    • 5-NITRONICOTINALDEHYDE
    • 5-nitropyridine-3-carbaldehyde
    • 5-Nitro-3-pyridinecarboxaldehyde (ACI)
    • Inchi： 1S/C6H4N2O3/c9-4-5-1-6(8(10)11)3-7-2-5/h1-4H
    • InChI Key： UJOOPEFUADGBNG-UHFFFAOYSA-N
    • SMILES： O=CC1C=C([N+](=O)[O-])C=NC=1

Computed Properties

  • Hydrogen Bond Donor Count: 0
  • Hydrogen Bond Acceptor Count: 2
  • Heavy Atom Count: 11
  • Rotatable Bond Count: 2

5-nitro-3-Pyridinecarboxaldehyde Pricemore >>

Related Categories No. Product Name Cas No. Purity Specification Price update time Inquiry
Alichem
A029005216-250mg
5-Nitronicotinaldehyde
 87883-20-3 95%
250mg
 $980.00 2023-08-31
Alichem
A029005216-500mg
5-Nitronicotinaldehyde
 87883-20-3 95%
500mg
 $1651.30 2023-08-31
Alichem
A029005216-1g
5-Nitronicotinaldehyde
 87883-20-3 95%
1g
 $2866.05 2023-08-31

5-nitro-3-Pyridinecarboxaldehyde Production Method

Production Method 1

Reaction Conditions
1.1 Reagents: Phosphoric acid Catalysts: Dicyclohexylcarbodiimide
Reference
Novel 1,4-dihydropyridine calcium antagonists. I. Synthesis and hypotensive activity of 4-(substituted pyridyl)-1,4-dihydropyridine derivatives
Ashimori, Atsuyuki; et al, Chemical & Pharmaceutical Bulletin, 1990, 38(9), 2446-58

Production Method 2

Reaction Conditions
1.1 Catalysts: Potassium carbonate
2.1 Reagents: Phosphoric acid Catalysts: Dicyclohexylcarbodiimide
Reference
Novel 1,4-dihydropyridine calcium antagonists. I. Synthesis and hypotensive activity of 4-(substituted pyridyl)-1,4-dihydropyridine derivatives
Ashimori, Atsuyuki; et al, Chemical & Pharmaceutical Bulletin, 1990, 38(9), 2446-58

Production Method 3

Reaction Conditions
Reference
Synthesis of 3-nitro-5-acylpyridines by condensation of sodium nitromalonaldehyde/tosyl chloride with 2-amino-1-acylolefins. Evidence for the intermediacy of 3-chloro-2-nitroacrolein
Hoffman, Jacob M.; et al, Journal of Organic Chemistry, 1984, 49(1), 193-5

Production Method 4

Reaction Conditions
1.1 Reagents: Phosphorus trichloride
2.1 Catalysts: Potassium carbonate
3.1 Reagents: Phosphoric acid Catalysts: Dicyclohexylcarbodiimide
Reference
Novel 1,4-dihydropyridine calcium antagonists. I. Synthesis and hypotensive activity of 4-(substituted pyridyl)-1,4-dihydropyridine derivatives
Ashimori, Atsuyuki; et al, Chemical & Pharmaceutical Bulletin, 1990, 38(9), 2446-58

Production Method 5

Reaction Conditions
1.1 Reagents: Silver nitrate
2.1 Reagents: Phosphorus trichloride
3.1 Catalysts: Potassium carbonate
4.1 Reagents: Phosphoric acid Catalysts: Dicyclohexylcarbodiimide
Reference
Novel 1,4-dihydropyridine calcium antagonists. I. Synthesis and hypotensive activity of 4-(substituted pyridyl)-1,4-dihydropyridine derivatives
Ashimori, Atsuyuki; et al, Chemical & Pharmaceutical Bulletin, 1990, 38(9), 2446-58

5-nitro-3-Pyridinecarboxaldehyde Raw materials

5-nitro-3-Pyridinecarboxaldehyde Preparation Products

5-nitro-3-Pyridinecarboxaldehyde Related Literature

87883-20-3 (5-nitro-3-Pyridinecarboxaldehyde) Related Products

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