Intermediate of API

872-85-5

  • Product Name:4-Pyridinecarboxaldehyde
  • Molecular Formula:C6H5NO
  • Specifications:99%
  • Molecular Weight:107.112
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Product Details;

CasNo: 872-85-5

Molecular Formula: C6H5NO

Appearance: clear yellow-brown liquid

Top Purity 4-Pyridinecarboxaldehyde 872-85-5 In Bulk Supply Best Price

  • Molecular Formula:C6H5NO
  • Molecular Weight:107.112
  • Appearance/Colour:clear yellow-brown liquid 
  • Vapor Pressure:0.492mmHg at 25°C 
  • Melting Point:-4--2 °C 
  • Refractive Index:n20/D 1.544(lit.)  
  • Boiling Point:192.3 °C at 760 mmHg 
  • PKA:12.05(at 30℃) 
  • Flash Point:54.4 °C 
  • PSA:29.96000 
  • Density:1.135 g/cm3 
  • LogP:0.89410 

4-Pyridinecarboxaldehyde(Cas 872-85-5) Usage

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.

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.]

InChI:InChI=1/C6H5NO/c8-5-6-1-3-7-4-2-6/h1-5H

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872-85-5 Process route

picoline
108-89-4

picoline

pyridine-4-carbaldehyde
872-85-5

pyridine-4-carbaldehyde

pyridine-4-carbonitrile
100-48-1

pyridine-4-carbonitrile

isonicotinamide
1453-82-3

isonicotinamide

Conditions
Conditions Yield
With manganese(IV) oxide; oxygen; urea; at 150 ℃; for 3h; under 3800.26 Torr; Autoclave;
78 %Chromat.
8 %Chromat.
52 %Chromat.
picoline
108-89-4

picoline

2,2'-diphenyl-[3,3']biindolylidene 1,1'-dioxide
2196-95-4,17213-48-8

2,2'-diphenyl-[3,3']biindolylidene 1,1'-dioxide

pyridine
110-86-1

pyridine

pyridine-4-carbaldehyde
872-85-5

pyridine-4-carbaldehyde

pyridine-4-carboxylic acid
55-22-1

pyridine-4-carboxylic acid

formaldehyd
50-00-0,30525-89-4,61233-19-0

formaldehyd

2,2'-diphenyl-1H,1'H-3,3'-biindole
2415-33-0

2,2'-diphenyl-1H,1'H-3,3'-biindole

Conditions
Conditions Yield
at 140 ℃; for 14h; Product distribution;
55%
13%
10%
31%

872-85-5 Upstream products

  • 108-89-4
    108-89-4

    picoline

  • 100-48-1
    100-48-1

    pyridine-4-carbonitrile

  • 586-95-8
    586-95-8

    pyridine-4-methanol

  • 3731-53-1
    3731-53-1

    4-(aminomethyl)pyridine

872-85-5 Downstream products

  • 13362-78-2
    13362-78-2

    trans-1,2-bis(pyridin-4-yl)ethene

  • 3515-49-9
    3515-49-9

    3-<4>Piperidylmethyl-indol

  • 23389-76-6
    23389-76-6

    4-hydroxypropylpyridine

  • 5061-42-7
    5061-42-7

    NL-19

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