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P33402

Sigma-Aldrich

2-Phenylpyridine

greener alternative

98%

Sinónimos:

α-Phenylpyridine, o-Phenylpyridine

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About This Item

Fórmula empírica (notación de Hill):
C11H9N
Número de CAS:
1008-89-5
Peso molecular:
155.20
Beilstein/REAXYS Number:
110445
EC Number:
213-763-1
MDL number:
MFCD00006280
UNSPSC Code:
12352100
PubChem Substance ID:
24898402
NACRES:
NA.22

assay

98%

greener alternative product score

old score: 2
new score: 1
Find out more about DOZN™ Scoring

greener alternative product characteristics

Atom Economy
Design for Energy Efficiency
Use of Renewable Feedstocks
Learn more about the Principles of Green Chemistry.

sustainability

Greener Alternative Product

refractive index

n20/D 1.623 (lit.)

bp

268-270 °C (lit.)

density

1.086 g/mL at 25 °C (lit.)

greener alternative category

Re-engineered,

SMILES string

c1ccc(cc1)-c2ccccn2

InChI

1S/C11H9N/c1-2-6-10(7-3-1)11-8-4-5-9-12-11/h1-9H

InChI key

VQGHOUODWALEFC-UHFFFAOYSA-N

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Categorías relacionadas

General description

We are committed to bringing you Greener Alternative Products, which adhere to one of the four categories of Greener Alternatives . This product belongs to category of Re-engineered products, showing key improvements in Green Chemistry Principles “Atom Economy”, “Design for Energy Efficiency” and “Use of Renewable Feedstock”. Click here to view its DOZN scorecard.

Application

Versatile synthetic intermediate.

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Referencia del producto
Descripción
Precios

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

10 - Combustible liquids

wgk_germany

WGK 3

flash_point_f

230.0 °F - closed cup

flash_point_c

110 °C - closed cup

ppe

Eyeshields, Gloves, type ABEK (EN14387) respirator filter

Certificados de análisis (COA)

Busque Certificados de análisis (COA) introduciendo el número de lote del producto. Los números de lote se encuentran en la etiqueta del producto después de las palabras «Lot» o «Batch»

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Huazhou Wu et al.
Dalton transactions (Cambridge, England : 2003), 40(9), 1969-1976 (2011-02-02)
Iridium(III) complexes with intense phosphorescence in solution have been widely applied in organic light-emitting diodes, chemosensors and bioimaging. However, little attention has been paid to iridium(III) complexes showing weak phosphorescence in solution and enhanced phosphorescence emission in the solid state
Michael T Vagnini et al.
Proceedings of the National Academy of Sciences of the United States of America, 109(39), 15651-15656 (2012-05-16)
Photodriving the activity of water-oxidation catalysts is a critical step toward generating fuel from sunlight. The design of a system with optimal energetics and kinetics requires a mechanistic understanding of the single-electron transfer events in catalyst activation. To this end
T Okada et al.
Journal of medicinal chemistry, 44(26), 4661-4667 (2001-12-14)
Mouse sarcoma 180 cell with a 25-fold higher cisplatin (CDDP) resistance, termed S-180cisR, is newly established. S-180cisR cells grow quite slowly in the presence of CDDP with high concentration. This may show that S-180cisR cells modulate the cell cycle to
Dik-Lung Ma et al.
Journal of the American Chemical Society, 131(5), 1835-1846 (2008-11-13)
A series of platinum(II) complexes containing dipyridophenazine (dppz) and C-deprotonated 2-phenylpyridine (N-CH) ligands were prepared and assayed for G-quadruplex DNA binding activities. [PtII(dppz-COOH)(N-C)]CF3SO3 (1; dppz-COOH = 11-carboxydipyrido[3,2-a:2',3'-c]phenazine) binds G-quadruplex DNA through an external end-stacking mode with a binding affinity of
Joeri Kuil et al.
Chembiochem : a European journal of chemical biology, 12(12), 1897-1903 (2011-07-09)
The chemokine receptor 4 (CXCR4) is over-expressed in 23 types of cancer in which it plays a role in, among others, the metastatic spread. For this reason it is a potential biomarker for the field of diagnostic oncology. The antagonistic
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