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856525

Sigma-Aldrich

2-Methyl-1,2-di-3-pyridyl-1-propanone

96%

Synonym(s):

Metyrapone, Su-4885

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About This Item

Empirical Formula (Hill Notation):
C14H14N2O
CAS Number:
Molecular Weight:
226.27
Beilstein/REAXYS Number:
163023
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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Quality Level

assay

96%

form

powder

mp

52-55 °C (lit.)

functional group

ketone

SMILES string

CC(C)(c1cccnc1)C(=O)c2cccnc2

InChI

1S/C14H14N2O/c1-14(2,12-6-4-8-16-10-12)13(17)11-5-3-7-15-9-11/h3-10H,1-2H3

InChI key

FJLBFSROUSIWMA-UHFFFAOYSA-N

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This Item
C5132
Carbazole ≥95% (GC)

C5132

Carbazole

assay

95%

assay

≥95% (GC)

Quality Level

100

Quality Level

200

mp

78-82 °C (lit.)

mp

243-246 °C (lit.)

functional group

hydroxyl

functional group

-

Application

2-Methyl-1,2-di-3-pyridyl-1-propanone inhibits the biosynthesis of corticosterone by blocking the conversion of deoxycorticosterone to corticosterone.[1] It is widely used in adrenocortical-related clinical studies.[2][3]

pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

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

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves


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Thermal aging of single-layer polymer light-emitting diodes composed of a carbazole and oxadiazole containing copolymer doped with singlet or triplet emitters.
Rungta P, et al.
Synthetic Metals, 160(23), 2486-2493 (2010)
Rukiye Ayranci et al.
The Analyst, 142(18), 3407-3415 (2017-08-22)
Herein, we report the synthesis and characterization of a new rhodamine-based monomer (RD-CZ), and an investigation of the optical and electrochemical properties of the corresponding polymer (P(RD-CZ)), which was electropolymerized on an ITO electrode. The resulting P(RD-CZ) polymer film was
Synthesis and photophysical properties of a poly (methyl methacrylate) polymer with carbazolyl side groups.
Martins TD, et al.
Journal of the Brazilian Chemical Society, 19(8), 1450-1461 (2008)
Yifen Lin et al.
Food chemistry, 264, 1-8 (2018-06-02)
Disassembly of cell wall polysaccharides accompanied with softening is very common in harvested fruits. To develop a facile postharvest approach, which can be used at ambient temperature, for suppressing softening and maintaining higher nutritive cell wall polysaccharides of Younai plums
Poly(methyl methacrylate)copolymers containing pendant carbazole and oxadiazole moieties for applications in single-layer organic light emitting devices.
Evanoff DD, et al.
Journal of Polymer Science Part A: Polymer Chemistry, 46(23), 7882-7897 (2008)

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