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142352

Sigma-Aldrich

4-Cyanopyridine N-oxide

96%

Synonym(s):

Isonicotinonitrile 1-oxide

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About This Item

Empirical Formula (Hill Notation):
C6H4N2O
CAS Number:
14906-59-3
Molecular Weight:
120.11
EC Number:
238-974-6
MDL number:
MFCD00006205
UNSPSC Code:
12352100
PubChem Substance ID:
24848520
NACRES:
NA.22

Assay

96%

form

solid

mp

223-225 °C (lit.)

solubility

1 M NH4OH: soluble 5 mg/mL, clear, colorless (methanol)

SMILES string

[O-][n+]1ccc(cc1)C#N

InChI

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

InChI key

QNCSFBSIWVBTHE-UHFFFAOYSA-N

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Classifications

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

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Zhao Xiang Yu et al.
Acta crystallographica. Section C, Crystal structure communications, 60(Pt 4), m194-m196 (2004-04-09)
The intermediate [Cd(4-PTZ)(2)(H(2)O)(4)] [4-PTZ is 5-(4-pyridyl N-oxide)tetrazolate, C(6)H(4)N(5)O], (I), in the synthesis of 4-HPTZ, (II), from the cycloaddition reaction of 4-cyanopyridine N-oxide with NaN(3) in water using CdCl(2) as catalyst, was structurally characterized. The unique Cd atom lies on a
Construction of Two Coordination Complexes Based on 5-(4-Pyridine N-oxide) Tetrazole (4-ptz) Generated by an in-situ [2+ 3] Cycloaddition Reaction.
Xiang J, et al.
Zeitschrift fur Anorganische und Allgemeine Chemie, 639(3-4), 563-568 (2013)
Carl M Blumenfeld et al.
Chemphyschem : a European journal of chemical physics and physical chemistry, 18(9), 1091-1100 (2017-01-18)
Globally scalable sunlight-driven devices that convert solar energy into storable fuels will require efficient light absorbers that are made of non-precious elements. Suitable photoanode materials are yet to be discovered. Here we utilised the timesaving nature of pulsed-laser-in-liquids synthesis and

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