P62208
3-Pyridinecarboxaldehyde
98%
Synonym(s):
Nicotinaldehyde
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About This Item
Empirical Formula (Hill Notation):
C6H5NO
CAS Number:
Molecular Weight:
107.11
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
207-900-4
Beilstein/REAXYS Number:
105343
MDL number:
Assay:
98%
InChI key
QJZUKDFHGGYHMC-UHFFFAOYSA-N
InChI
1S/C6H5NO/c8-5-6-2-1-3-7-4-6/h1-5H
SMILES string
[H]C(=O)c1cccnc1
assay
98%
Quality Level
refractive index
n20/D 1.549 (lit.)
bp
78-81 °C/10 mmHg (lit.)
density
1.141 g/mL at 20 °C (lit.)
storage temp.
2-8°C
Related Categories
signalword
Warning
Hazard Classifications
Acute Tox. 4 Oral - Aquatic Chronic 3 - Flam. Liq. 3 - Skin Irrit. 2 - Skin Sens. 1 - STOT SE 3
target_organs
Respiratory system
Storage Class
3 - Flammable liquids
wgk
WGK 3
flash_point_f
95.0 °F - closed cup
flash_point_c
35 °C - closed cup
ppe
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
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K S De Jongh et al.
The Biochemical journal, 242(1), 143-150 (1987-02-15)
The kinetic mechanism of the major sheep liver aldehyde reductase (ALR1) was studied with three aldehyde substrates: p-nitrobenzaldehyde, pyridine-3-aldehyde and D-glucuronate. In each case the enzyme mechanism was sequential and product-inhibition studies were consistent with an ordered Bi Bi mechanism
P Narender et al.
Bioorganic & medicinal chemistry letters, 15(24), 5378-5381 (2005-10-11)
New Baylis-Hillman adducts are synthesized based on substituted 2-chloronicotinaldehydes and screened for their in vitro anti-malarial activity against chloroquine sensitive and chloroquine resistant Plasmodium falciparum. Out of the six new compounds synthesized and screened, 2b, 2c and 2d compounds showed
[Selenazoles. IX. [9]. 3-methyl-4-R-selenazolidene-2-hydrazones of acetaldehyde, benzaldehyde, isonicotinaldehyde, nicotinaldehyde and picolinaldehyde].
S Biliński et al.
Annales Universitatis Mariae Curie-Sklodowska. Sectio D: Medicina, 39, 25-31 (1984-01-01)
Sujin P Jose et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 64(1), 205-209 (2006-03-18)
The Fourier transform Raman and infrared spectra of nicotinaldehyde were recorded and the observed frequencies were assigned to various modes of vibration in terms of fundamentals by assuming Cs point group symmetry. A normal coordinate analysis was also carried out
C C Shone et al.
Biochemistry, 20(26), 7494-7501 (1981-12-22)
Coenzyme A linked aldehyde dehydrogenase from Escherichia coli strain B has been purified to a specific activity of 14 units/mg of protein, and initial rate and substrate analogue inhibition experiments have been performed. On the basis of these steady-state measurements
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