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D216305

Sigma-Aldrich

2,2′-Bipyridyl

greener alternative

ReagentPlus®, ≥99%

Sinonimo/i:

2,2′-Bipyridine, 2,2′-Dipyridine, 2,2′-Dipyridyl

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About This Item

Formula empirica (notazione di Hill):
C10H8N2
Numero CAS:
Peso molecolare:
156.18
Beilstein:
113089
Numero CE:
Numero MDL:
Codice UNSPSC:
12352100
ID PubChem:
NACRES:
NA.21

Origine biologica

synthetic (organic)

Livello qualitativo

Nome Commerciale

ReagentPlus®

Saggio

≥99%

Forma fisica

powder or crystals
powder or granules

Caratteristiche più verdi

Catalysis
Learn more about the Principles of Green Chemistry.

sustainability

Greener Alternative Product

P. eboll.

273 °C (lit.)

Punto di fusione

70-73 °C (lit.)

Solubilità

ethanol: 100 mg/mL, clear, colorless to faintly yellow

Categoria alternativa più verde

Temperatura di conservazione

room temp

Stringa SMILE

c1ccc(nc1)-c2ccccn2

InChI

1S/C10H8N2/c1-3-7-11-9(5-1)10-6-2-4-8-12-10/h1-8H
ROFVEXUMMXZLPA-UHFFFAOYSA-N

Informazioni sul gene

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Descrizione generale

2,2′-Bipyridyl also known as 2,2′-bipyridine, is a symmetrical bipyridine commonly used as a neutral ligand for chelating with metal ions. It is a bidentate ligand which has been employed transition metal catalysis, aluminum initiated polymerization, and various other inorganic syntheses. This compound adheres to the principles of greener chemistry, ensuring catalytic efficiency. Click here for more information

Applicazioni

2,2′-Bipyridyl has been used in:
  • the preparation of fluorescent dyes like products 754730, 544981, 804215.
  • the preparation ofcopper(II)-bipyridine-naringenin complex.
  • the preparation of 2,2′-bipyridyl hydrobromide.
  • as a ligand in the greener oxidation of alcohols under aerobic conditions
  • as a complex with CuBR2 in the green synthesis of propargylamines
  • the synthesis of [Ru(bipy)3]Cl2, a common metal complex with usefulphotochemistry often used in photoredox catalysis as a sensitizer

Azioni biochim/fisiol

Metalloprotease inhibitor, high-affinity chelator of iron; may inhibit Fe2+ containing enzymes at 10−8 M.

Note legali

ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany

Pittogrammi

Skull and crossbones

Avvertenze

Danger

Indicazioni di pericolo

Classi di pericolo

Acute Tox. 3 Dermal - Acute Tox. 3 Oral

Codice della classe di stoccaggio

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

267.8 °F - closed cup

Punto d’infiammabilità (°C)

131 °C - closed cup

Dispositivi di protezione individuale

Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges


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I clienti hanno visto anche

Slide 1 of 2

1 of 2

Macromolecules, 27, 645-645 (1994)
Bromination of 2,2'-bipyridile.
Zdravkov AB and Khimich NN.
Russ. J. Org. Chem., 42(8), 1200-1202 (2006)
Júlio César Conceição Filho et al.
PloS one, 9(9), e107058-e107058 (2014-09-06)
Cancer is the second leading cause of death worldwide and there is epidemiological evidence that demonstrates this tendency is emerging. Naringenin (NGEN) is a trihydroxyflavanone that shows various biological effects such as antioxidant, anticancer, anti-inflammatory, and antiviral activities. It belongs
Tetrahedron Letters, 34, 6219-6219 (1993)
Organic Photoredox Catalysis
Nathan A Romero
Chemical Reviews, 116(17), 10075?10166-10075?10166 (2016)

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