2402-98-4

  • Product Name:2-cyanopyridine-N-oxide
  • Molecular Formula:C6H4 N2 O
  • Purity:99%
  • Molecular Weight:120.111
Inquiry

Product Details

pd_meltingpoint:123-124 °C

Purity:99%

Perfect Factory Offer Excellent quality 2-cyanopyridine-N-oxide 2402-98-4 with Safe Shipping

  • Molecular Formula:C6H4 N2 O
  • Molecular Weight:120.111
  • Vapor Pressure:4.63E-06mmHg at 25°C 
  • Melting Point:123-124 °C 
  • Boiling Point:382.7°Cat760mmHg 
  • PKA:-1.92±0.10(Predicted) 
  • Flash Point:185.3°C 
  • PSA:49.25000 
  • Density:1.14g/cm3 
  • LogP:0.98678 

pyridine-2-carbonitrile 1-oxide(Cas 2402-98-4) Usage

General Description

Pyridine-2-carbonitrile 1-oxide is a chemical compound with the molecular formula C6H4N2O. It is a nitrogen-containing heterocyclic compound that contains a pyridine ring and a nitrile group. The 1-oxide functionality indicates the presence of an oxygen atom attached to the first position of the pyridine ring. pyridine-2-carbonitrile 1-oxide is used in various chemical reactions and synthesis processes, and it has potential applications in pharmaceuticals and agrochemicals. It is important to handle pyridine-2-carbonitrile 1-oxide with caution, as it may have hazardous properties and should be used in a controlled and safe manner.

InChI:InChI=1/C6H4N2O/c7-5-6-3-1-2-4-8(6)9/h1-4H

2402-98-4 Relevant articles

Regioselective Three-Component Reaction of Pyridine N-Oxides, Acyl Chlorides, and Cyclic Ethers

Jones, D. Heulyn,Kay, Steven T.,McLellan, Jayde A.,Kennedy, Alan R.,Tomkinson, Nicholas C. O.

supporting information, p. 3512 - 3515 (2017/07/17)

A novel three-component reaction of pyri...

Catalyst-free and selective oxidation of pyridine derivatives and tertiary amines to corresponding N-oxides with 1,2-diphenyl-1,1,2,2-tetrahydroperoxyethane

Azarifar, Davood,Mahmoudi, Boshra

, p. 645 - 651 (2016/02/19)

The catalyst-free oxidation of various p...

Solvent- and halide-free synthesis of pyridine-2-yl substituted ureas through facile C-H functionalization of pyridine: N -oxides

Rassadin, Valentin A.,Zimin, Dmitry P.,Raskil'dina, Gulnara Z.,Ivanov, Alexander Yu.,Boyarskiy, Vadim P.,Zlotskii, Semen S.,Kukushkin, Vadim Yu.

supporting information, p. 6630 - 6636 (2018/03/01)

A novel solvent- and halide-free atom-ec...

Base free regioselective synthesis of α-triazolylazine derivatives

Harisha, Mysore Bhyrappa,Nagaraj, Muthupandi,Muthusubramanian, Shanmugam,Bhuvanesh, Nattamai

, p. 58118 - 58124 (2016/07/06)

A regioselective α-heteroarylation follo...

2402-98-4 Process route

(Z)-2-pyridinecarbaldehyde 1-oxide oxime
24145-26-4

(Z)-2-pyridinecarbaldehyde 1-oxide oxime

pyridine-2-carboxylic acid amide
1452-77-3

pyridine-2-carboxylic acid amide

(E)-2-pyridinecarbaldehyde 1-oxide oxime
24145-28-6

(E)-2-pyridinecarbaldehyde 1-oxide oxime

2-cyanopyridine N-oxide
2402-98-4

2-cyanopyridine N-oxide

2-pyridinecarboxamide 1-oxide
6974-72-7

2-pyridinecarboxamide 1-oxide

Conditions
Conditions Yield
With C5H11OH; ammonium chloride; sodium amide; isopentyl nitrite; In ammonia; Ambient temperature;
40%
14%
12%
5%
2-Cyanopyridine
100-70-9,1232006-36-8

2-Cyanopyridine

2-cyanopyridine N-oxide
2402-98-4

2-cyanopyridine N-oxide

Conditions
Conditions Yield
With dihydrogen peroxide; methyltrioxorhenium(VII); In dichloromethane; water; at 20 ℃; Inert atmosphere;
100%
With HOF* CH3CN; In chloroform; at 0 - 20 ℃;
98%
With dihydrogen peroxide; methyltrioxorhenium(VII); In dichloromethane; water; for 24h; Ambient temperature;
94%
With 1,2-diphenyl-1,1,2,2-tetrahydroperoxyethane; In acetonitrile; at 20 ℃; for 0.0833333h;
93%
With bis-trimethylsilanyl peroxide; per-rhenic acid; In dichloromethane; water; at 24 ℃; for 15h;
92%
With 3-chloro-benzenecarboperoxoic acid; In dichloromethane; for 24h; Inert atmosphere;
88%
With titanium silicate; dihydrogen peroxide; In methanol; at 60 ℃; for 25h;
81.3%
With oxygen; isobutyraldehyde; In 1,2-dichloro-ethane; at 30 ℃; for 24h;
76%
With oxygen; ruthenium trichloride; In 1,2-dichloro-ethane; at 20 ℃; for 20h; under 760 Torr;
75%
With dihydrogen peroxide; acetic anhydride; In water; at 80 ℃; for 12h;
62%
With 3-chloro-benzenecarboperoxoic acid; In dichloromethane; at 20 ℃;
56%
With dihydrogen peroxide; acetic acid;
2-Cyanopyridine; With dihydrogen peroxide; methyltrioxorhenium(VII); In dichloromethane; water; at 20 ℃; for 6h;
manganese(IV) oxide; In dichloromethane; water; at 20 ℃; for 1h;
With 3-chloro-benzenecarboperoxoic acid; In dichloromethane;

2402-98-4 Upstream products

  • 100-70-9
    100-70-9

    2-Cyanopyridine

  • 6974-72-7
    6974-72-7

    2-pyridinecarboxamide 1-oxide

  • 24145-26-4
    24145-26-4

    (Z)-2-pyridinecarbaldehyde 1-oxide oxime

  • 1452-77-3
    1452-77-3

    pyridine-2-carboxylic acid amide

2402-98-4 Downstream products

  • 100-70-9
    100-70-9

    2-Cyanopyridine

  • 1192-31-0
    1192-31-0

    cis-2,3-epoxy-4-methylpentane

  • 1192-31-0
    1192-31-0

    trans-2,3-epoxy-4-methylpentane

  • 72221-03-5
    72221-03-5

    2,3-dimethyl-1,2-epoxybutane