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Key Documents

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P62208

Sigma-Aldrich

3-Pyridinecarboxaldehyde

98%

Sinónimos:

Nicotinaldehyde

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About This Item

Fórmula empírica (notación de Hill):
C6H5NO
Número de CAS:
500-22-1
Peso molecular:
107.11
Beilstein/REAXYS Number:
105343
EC Number:
207-900-4
MDL number:
MFCD00006382
UNSPSC Code:
12352100
PubChem Substance ID:
24898656
NACRES:
NA.22

Quality Level

200

assay

98%

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

SMILES string

[H]C(=O)c1cccnc1

InChI

1S/C6H5NO/c8-5-6-2-1-3-7-4-6/h1-5H

InChI key

QJZUKDFHGGYHMC-UHFFFAOYSA-N

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pictograms

FlameExclamation mark
GHS02,GHS07

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_germany

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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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
[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)
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
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
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
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