Ethyl 2-acetylhexanoate

Base Information

  • Chemical Name: Ethyl 2-acetylhexanoate
  • CAS No.: 1540-29-0

Factory supply Ethyl 2-acetylhexanoate 1540-29-0 with sufficient production capacity

  • Molecular Formula: C10H18O3
  • Molecular Weight: 186.251
  • Appearance/Colour: transparent oily liquid 
  • Vapor Pressure: 0.107mmHg at 25°C 
  • Refractive Index: 1.4320 
  • Boiling Point: 221.5 ºC at 760 mmHg 
  • PKA: 12.32±0.46(Predicted) 
  • Flash Point: 89.1 ºC 
  • PSA： 43.37000 
  • Density: 0.957 g/cm3 
  • LogP: 1.94490 

Ethyl 2-acetylhexanoate(Cas 1540-29-0) Usage

Synthesis Reference(s)

Journal of the American Chemical Society, 64, p. 580, 1942 DOI: 10.1021/ja01255a035Synthetic Communications, 24, p. 111, 1994 DOI: 10.1080/00397919408012633

InChI:InChI=1/C10H18O3/c1-4-6-7-9(8(3)11)10(12)13-5-2/h9H,4-7H2,1-3H3

1540-29-0 Relevant articles

Synthesis of some disubstituted cyanoacetamides as potential anticonvulsants.

Schwartz 2nd.,Worrell,Delgado

, p. 80 - 86 (1967)

-

Synthesis and fungicidal activities of perfluoropropan-2-yl-based novel quinoline derivatives

Zhang, Zai,Liu, Minhua,Liu, Weidong,Xiang, Jun,Li, Jianming,Li, Zhong,Liu, Xingping,Huang, Mingzhi,Liu, Aiping,Zheng, Xingliang

, p. 91 - 97 (2019)

A series of novel perfluoropropan-2-yl-b...

Synthetic Scope of Br?nsted Acid-Catalyzed Reactions of Carbonyl Compounds and Ethyl Diazoacetate

Rahaman, Mizzanoor,Ali, M. Shahnawaz,Jahan, Khorshada,Hinz, Damon,Belayet, Jawad Bin,Majinski, Ryan,Hossain, M. Mahmun

, p. 6138 - 6147 (2021/05/06)

The comprehensive study of the reactions...

Nano-K2CO3: Preparation, characterization and evaluation of reactive activities

Li, Jun-Zhang,Fan, Shi-Ming,Sun, Xuan-Fei,Liu, Shouxin

, p. 1865 - 1869 (2016/01/20)

A novel base, nano-K2CO3, was easily pre...

Rh(I)-bisphosphine-catalyzed asymmetric, intermolecular hydroheteroarylation of α-substituted acrylate derivatives

Filloux, Claire M.,Rovis, Tomislav

supporting information, p. 508 - 517 (2015/01/30)

Asymmetric hydroheteroarylation of alken...

1540-29-0 Process route

1-bromo-butane
109-65-9

1-bromo-butane

ethyl acetoacetate
141-97-9

ethyl acetoacetate

ethyl 2-butylacetoacetate
1540-29-0

ethyl 2-butylacetoacetate

Conditions
Conditions Yield
With potassium carbonate; In ethanol; water; at 70 ℃; for 10h; regioselective reaction;
83.2%
With potassium carbonate; In N,N-dimethyl-formamide; for 0.0333333h; microwave irradiation;
70%
With potassium hydroxide; tetrabutyl-ammonium chloride; potassium carbonate; for 0.075h; Irradiation;
61%
With potassium 2-methylbutan-2-olate;
With sodium hydroxide; ethanol;
With potassium hydroxide; acetaldehyde dipropyl acetal;
With sodium hydride; tetramethylurea;
With potassium hydroxide; In formamide;
Multistep reaction; (i) aq. KOH, (ii) /BRN= 1098260/;
With sodium ethanolate; In ethanol; at 23 ℃; for 24h; Reflux; Inert atmosphere;
1-bromo-butane
109-65-9

1-bromo-butane

sodium ethyl acetylacetate enolate
1007476-32-5

sodium ethyl acetylacetate enolate

ethyl 2-butylacetoacetate
1540-29-0

ethyl 2-butylacetoacetate

Conditions
Conditions Yield
unter verschiedenen Bedingungen;
With ethanol;
at 95 - 105 ℃;

1540-29-0 Upstream products

  • 109-65-9
    109-65-9

    1-bromo-butane

  • 1007476-32-5
    1007476-32-5

    sodium ethyl acetylacetate enolate

  • 141-97-9
    141-97-9

    ethyl acetoacetate

  • 623-73-4
    623-73-4

    diazoacetic acid ethyl ester

1540-29-0 Downstream products

  • 29113-41-5
    29113-41-5

    5-butyl-6-methyl-2-thiouracil

  • 857939-30-1
    857939-30-1

    (+/-)-2-butyl-3-(4-bromo-phenyl)-propionic acid

  • 108299-22-5
    108299-22-5

    3-butyl-5-hydroxy-4,7-dimethyl-coumarin

  • 111-65-9
    111-65-9

    octane

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