59146-67-7

  • Product Name:2-Cyano-5,6-dimethylpyridine
  • Molecular Formula:C8H8N2
  • Purity:99%
  • Molecular Weight:132.16
Inquiry

Product Details

Purity:99%

Purity 99% Min 2-Cyano-5,6-dimethylpyridine 59146-67-7 Spot Supply with Safe Transportation

  • Molecular Formula:C8H8N2
  • Molecular Weight:132.16
  • Boiling Point:280.7±35.0 °C(Predicted) 
  • PKA:0.69±0.10(Predicted) 
  • PSA:36.68000 
  • Density:1.05±0.1 g/cm3(Predicted) 
  • LogP:1.57008 

59146-67-7 Relevant articles

SUBSTITUTED PYRIDIZINONE DERIVATIVES AS PDE10 INHIBITORS

-

Page/Page column 57, (2014/09/29)

The present invention is directed to sub...

SUBSTITUTED PYRIDIZINONE DERIVATIVES AS PDE10 INHIBITORS

-

Page/Page column 57, (2014/10/04)

The present invention is directed to sub...

5-lipoxygenase-activating protein (FLAP) inhibitors. Part 4: Development of 3-[3-tert-butylsulfanyl-1-[4-(6-ethoxypyridin-3-yl)benzyl]-5-(5-methylpyridin- 2-ylmethoxy)-1 H -indol-2-yl]-2,2-dimethylpropionic acid (AM803), a potent, oral, once daily FLAP inhibitor

Stock, Nicholas S.,Bain, Gretchen,Zunic, Jasmine,Li, Yiwei,Ziff, Jeannie,Roppe, Jeffrey,Santini, Angelina,Darlington, Janice,Prodanovich, Pat,King, Christopher D.,Baccei, Christopher,Lee, Catherine,Rong, Haojing,Chapman, Charles,Broadhead, Alex,Lorrain, Dan,Correa, Lucia,Hutchinson, John H.,Evans, Jilly F.,Prasit, Peppi

experimental part, p. 8013 - 8029 (2012/03/08)

The potent 5-lipoxygenase-activating pro...

BENZOXAZINONE DERIVATIVES FOR THE TREATMENT OF GLYTL MEDIATED DISORDERS

-

Page/Page column 63; 64, (2011/02/24)

The present invention relates to benzoxa...

59146-67-7 Process route

2,3-dimethylpyridine 1-oxide
22710-07-2,166521-76-2

2,3-dimethylpyridine 1-oxide

trimethylsilyl cyanide
7677-24-9

trimethylsilyl cyanide

5,6-dimethylpyridine-2-carbonitrile
59146-67-7

5,6-dimethylpyridine-2-carbonitrile

Conditions
Conditions Yield
With N,N-Dimethylcarbamoyl chloride; In dichloromethane; at 20 ℃; for 72h;
75%
With N,N-diethylcarbamyl chloride; In dichloromethane; at 20 ℃; for 60h; Inert atmosphere;
53%
With N,N-diethylcarbamyl chloride; In 1,2-dichloro-ethane; Ambient temperature;
2,3-dimethylpyridine 1-oxide; trimethylsilyl cyanide; With triethylamine; In acetonitrile; at 90 ℃; for 120h; Inert atmosphere;
With sodium hydroxide; In water; acetonitrile; at 0 ℃;
2,3-dimethylpyridine 1-oxide; trimethylsilyl cyanide; In dichloromethane; at 20 ℃; for 0.5h;
With N,N-diethylcarbamyl chloride; In dichloromethane; at 20 ℃; for 24h;
2,3-dimethylpyridine 1-oxide; trimethylsilyl cyanide; In dichloromethane; at 20 ℃; for 0.5h;
With N,N-diethylcarbamyl chloride; In dichloromethane; for 24h;
aq. K2 CO3

aq. K2 CO3

diethyl ether
60-29-7,927820-24-4

diethyl ether

trimethylsilyl cyanide
7677-24-9

trimethylsilyl cyanide

N,N-diethylcarbamyl chloride
88-10-8

N,N-diethylcarbamyl chloride

5,6-dimethylpyridine-2-carbonitrile
59146-67-7

5,6-dimethylpyridine-2-carbonitrile

Conditions
Conditions Yield
In dichloromethane;

59146-67-7 Upstream products

  • 22710-07-2
    22710-07-2

    2,3-dimethylpyridine 1-oxide

  • 7677-24-9
    7677-24-9

    trimethylsilyl cyanide

  • 60-29-7
    60-29-7

    diethyl ether

  • 88-10-8
    88-10-8

    N,N-diethylcarbamyl chloride

59146-67-7 Downstream products

  • 543713-56-0
    543713-56-0

    (5,6-dimethylpyridin-2-yl)methanamine

  • 153646-65-2
    153646-65-2

    2-hydroxymethyl-5,6-dimethylpyridine

  • 83282-49-9
    83282-49-9

    5,6-dimethyl-pyridine-2-carboxylic acid