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6-methyl-2,2'-bipyridine

Names

[ CAS No. ]:
56100-22-2

[ Name ]:
6-methyl-2,2'-bipyridine

[Synonym ]:
6-Methyl-2,2'dipyridine
6-methyl-2,2'-bipyridine
6-methyl-2-(2-pyridyl)pyridine
6-Methyl-2,2'-dipyridyl
MFCD02093688
2,2'-bipyridine,6-methyl
6-Methyl-[2,2']bipyridinyl
2-methyl-6-(pyridin-2-yl)pyridine

Chemical & Physical Properties

[ Density]:
1.09 g/mL at 25ºC(lit.)

[ Boiling Point ]:
117-119ºC0.1 mm Hg(lit.)

[ Molecular Formula ]:
C11H10N2

[ Molecular Weight ]:
170.21000

[ Flash Point ]:
>230 °F

[ Exact Mass ]:
170.08400

[ PSA ]:
25.78000

[ LogP ]:
2.45200

[ Index of Refraction ]:
n20/D 1.607(lit.)

MSDS

Safety Information

[ Symbol ]:

GHS07

[ Signal Word ]:
Warning

[ Hazard Statements ]:
H315-H319-H335

[ Precautionary Statements ]:
P261-P305 + P351 + P338

[ Personal Protective Equipment ]:
Eyeshields;full-face respirator (US);Gloves;multi-purpose combination respirator cartridge (US);type ABEK (EN14387) respirator filter

[ Hazard Codes ]:
Xi

[ Risk Phrases ]:
36/37/38

[ Safety Phrases ]:
26-36

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

[ HS Code ]:
2933399090

Precursor & DownStream

Customs

[ HS Code ]: 2933399090

[ Summary ]:
2933399090. other compounds containing an unfused pyridine ring (whether or not hydrogenated) in the structure. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

Articles

Palladium(II)-catalyzed desulfitative synthesis of aryl ketones from sodium arylsulfinates and nitriles: scope, limitations, and mechanistic studies.

J. Org. Chem. 79(24) , 12018-32, (2014)

A fast and efficient protocol for the palladium(II)-catalyzed production of aryl ketones from sodium arylsulfinates and various organic nitriles under controlled microwave irradiation has been develop...

Chemical Constitution and Activity of Bipyridylium Herbicides. XII. Diquaternary Salts of 6-Methyl-2, 2'-bipyridyl and 2-Methyl-4, 4'-bipyridyl. Schmalzl K and Summers L.

Aust. J. Chem. 30(3) , 657-662, (1977)

Efficient synthesis of 4-, 5-, and 6-methyl-2, 2'-bipyridine by a Negishi cross-coupling strategy followed by high-yield conversion to bromo-and chloromethyl-2, 2'-bipyridines. Savage SA, et al.

J. Org. Chem. 63(26) , 10048-10051, (1998)


More Articles


Related Compounds

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