Ethyl 2-methylnicotinate


  • CasNo 1721-26-2
  • Purity 99%
Inquery

Manufacturer supply good quality Ethyl 2-methylnicotinate 1721-26-2 with stock

  • Molecular Formula: C9H11NO2
  • Molecular Weight: 165.192
  • Vapor Pressure: 0.0521mmHg at 25°C 
  • Melting Point: 146-147 °C 
  • Refractive Index: n20/D 1.505(lit.)  
  • Boiling Point: 234.704 °C at 760 mmHg 
  • PKA: 4.02±0.10(Predicted) 
  • Flash Point: 86.031 °C 
  • PSA: 39.19000 
  • Density: 1.077 g/cm3 
  • LogP: 1.56670 

Ethyl 2-methylnicotinate(Cas 1721-26-2) Usage

InChI:InChI=1/C9H11NO2/c1-3-12-9(11)8-5-4-6-10-7(8)2/h4-6H,3H2,1-2H3

1721-26-2 Relevant articles

Intramolecular alkylations of aromatic compounds, XII: Synthesis of 1-(3-methylpyridin-2-ylmethyl)-1,2,3,4-tetrahydronaphthalenes

Reimann,Bauer

, p. 879 - 887 (1983)

-

A heavy metal- and oxidant-free, one-pot synthesis of pyridines and fused pyridines based on a Lewis acid-catalyzed multicomponent reaction

Raja, V. P. Alex,Tenti, Giammarco,Perumal, Subbu,Menndez, J. Carlos

, p. 12270 - 12272 (2014)

The InCl3-catalyzed sequential multicomp...

Method for preparing 2 -methylnicotinate and derivatives thereof

-

, (2021/12/07)

The invention belongs to the technical f...

Sonochemical synthesis of 2-substituted nicotinic acid ethyl ester derivatives: Their in vitro and in silico evaluation against SIRT1

Challa, Chandra Sekhar,Kapavarapu, Ravikumar,Katari, Naresh Kumar,Nallanchakravarthula, Varadacharyulu,Nayakanti, Devanna,Pal, Manojit

, (2021/07/27)

Based on the initial docking studies of ...

2-methyl nicotinate as well as preparation method and application thereof

-

Paragraph 0114-0146, (2021/05/22)

The invention relates to 2-methyl nicoti...

Transition-Metal-Free Synthesis of Pyridine Derivatives by Thermal Cyclization of N -Propargyl Enamines

Chikayuki, Yuya,Higashiyama, Kimio,Kirita, Akiko,Matsuo, Natsuko,Miyashige, Takakane,Sasaki, Shigeru,Teramoto, Hiroyoshi,Yamauchi, Takayasu,Yonekawa, Shiori

, p. 1113 - 1121 (2020/04/01)

A transition-metal-free synthesis of pyr...

1721-26-2 Process route

1-methylpyrimidin-1-ium iodide
60544-22-1

1-methylpyrimidin-1-ium iodide

ethyl (E)-3-aminobut-2-enoate
41867-20-3

ethyl (E)-3-aminobut-2-enoate

ethyl 2-methyl nicotinate
1721-26-2

ethyl 2-methyl nicotinate

2,6-dimethyl-pyridine-3,5-dicarboxylic acid diethyl ester
1149-24-2

2,6-dimethyl-pyridine-3,5-dicarboxylic acid diethyl ester

diethyl 1,4-dihydro-2,4,6-trimethylpyridine-3,5-dicarboxylate
632-93-9

diethyl 1,4-dihydro-2,4,6-trimethylpyridine-3,5-dicarboxylate

Conditions
Conditions Yield
In pyridine; for 6h; Heating;
3%
3%
25%
1-methylpyrimidin-1-ium iodide
60544-22-1

1-methylpyrimidin-1-ium iodide

ethyl N-methyl-β-aminocrotonate
21759-71-7

ethyl N-methyl-β-aminocrotonate

ethyl 2-methyl nicotinate
1721-26-2

ethyl 2-methyl nicotinate

2,6-dimethyl-pyridine-3,5-dicarboxylic acid diethyl ester
1149-24-2

2,6-dimethyl-pyridine-3,5-dicarboxylic acid diethyl ester

diethyl 1,4-dihydro-2,4,6-trimethylpyridine-3,5-dicarboxylate
632-93-9

diethyl 1,4-dihydro-2,4,6-trimethylpyridine-3,5-dicarboxylate

Conditions
Conditions Yield
In pyridine; for 6h; Heating;
1%
1%
8%

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1721-26-2 Downstream products

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    7-phenyl-7,8-dihydro-pyrano[4,3-b ]pyridin-5-one

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    56826-61-0

    (2-methylpyridin-3-yl)methanol

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